Autoimmune lymphoproliferative syndrome: Difference between revisions
Line 24: | Line 24: | ||
==[[Autoimmune lymphoproliferative syndrome overview|Overview]]== | ==[[Autoimmune lymphoproliferative syndrome overview|Overview]]== | ||
== [[Autoimmune lymphoproliferative syndrome historical perspective|Historical Perspective]] == | ==[[Autoimmune lymphoproliferative syndrome historical perspective|Historical Perspective]]== | ||
== Discovery == | |||
==== Overview[edit | edit source] ==== | |||
==== Historical Perspective[edit | edit source] ==== | |||
==== References ==== | |||
==Discovery== | |||
<br /> | |||
== Overview == | |||
The exact pathogenesis of [disease name] is not fully understood. | |||
OR | |||
It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3]. | |||
OR | |||
[Pathogen name] is usually transmitted via the [transmission route] route to the human host. | |||
OR | |||
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell. | |||
OR | |||
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells]. | |||
OR | |||
The progression to [disease name] usually involves the [molecular pathway]. | |||
OR | |||
The pathophysiology of [disease/malignancy] depends on the histological subtype. | |||
== Pathophysiology == | |||
=== Physiology === | |||
The normal physiology of [name of process] can be understood as follows: | |||
=== Pathogenesis === | |||
* The exact pathogenesis of [disease name] is not completely understood. | |||
OR | |||
* It is understood that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3]. | |||
* [Pathogen name] is usually transmitted via the [transmission route] route to the human host. | |||
* Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell. | |||
* [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells]. | |||
* The progression to [disease name] usually involves the [molecular pathway]. | |||
* The pathophysiology of [disease/malignancy] depends on the histological subtype. | |||
== Genetics == | |||
[Disease name] is transmitted in [mode of genetic transmission] pattern. | |||
OR | |||
Genes involved in the pathogenesis of [disease name] include: | |||
* [Gene1] | |||
* [Gene2] | |||
* [Gene3] | |||
OR | OR | ||
The development of [disease name] is the result of multiple genetic mutations such as: | |||
The | |||
References | * [Mutation 1] | ||
* [Mutation 2] | |||
* [Mutation 3] | |||
== Associated Conditions == | |||
Conditions associated with [disease name] include: | |||
* [Condition 1] | |||
* [Condition 2] | |||
* [Condition 3] | |||
== Gross Pathology == | |||
On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name]. | |||
== Microscopic Pathology == | |||
On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name]. | |||
== References == | |||
==[[Autoimmune lymphoproliferative syndrome classification|Classification]]== | ==[[Autoimmune lymphoproliferative syndrome classification|Classification]]== | ||
<br /> | |||
== Overview == | |||
There is no established system for the classification of [disease name]. | |||
OR | |||
[Disease name] may be classified according to [classification method] into [number] subtypes/groups: [group1], [group2], [group3], and [group4]. | |||
OR | |||
[Disease name] may be classified into [large number > 6] subtypes based on [classification method 1], [classification method 2], and [classification method 3]. [Disease name] may be classified into several subtypes based on [classification method 1], [classification method 2], and [classification method 3]. | |||
OR | |||
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic. | |||
OR | |||
If the staging system involves specific and characteristic findings and features: According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2]. | |||
OR | |||
The staging of [malignancy name] is based on the [staging system]. | |||
OR | |||
There is no established system for the staging of [malignancy name]. | |||
== Classification == | |||
There is no established system for the classification of [disease name]. | |||
OR | |||
[Disease name] may be classified according to [classification method] into [number] subtypes/groups: | |||
* [Group1] | |||
* [Group2] | |||
* [Group3] | |||
* [Group4] | |||
OR | |||
[Disease name] may be classified into [large number > 6] subtypes based on: | |||
* [Classification method 1] | |||
* [Classification method 2] | |||
* [Classification method 3] | |||
[Disease name] may be classified into several subtypes based on: | |||
* [Classification method 1] | |||
* [Classification method 2] | |||
* [Classification method 3] | |||
OR | |||
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic. | |||
OR | |||
'''If the staging system involves specific and characteristic findings and features:''' | |||
According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2]. | |||
OR | |||
The staging of [malignancy name] is based on the [staging system]. | |||
OR | |||
There is no established system for the staging of [malignancy name]. | |||
== References == | |||
==[[Autoimmune lymphoproliferative syndrome pathophysiology|Pathophysiology]]== | ==[[Autoimmune lymphoproliferative syndrome pathophysiology|Pathophysiology]]== | ||
<br /> | |||
== Overview == | |||
The exact pathogenesis of [disease name] is not fully understood. | |||
OR | |||
It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3]. | |||
OR | |||
[Pathogen name] is usually transmitted via the [transmission route] route to the human host. | |||
OR | |||
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell. | |||
OR | |||
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells]. | |||
OR | |||
The progression to [disease name] usually involves the [molecular pathway]. | |||
OR | |||
The pathophysiology of [disease/malignancy] depends on the histological subtype. | |||
== Pathophysiology == | |||
=== Physiology === | |||
The normal physiology of [name of process] can be understood as follows: | |||
=== Pathogenesis === | |||
* The exact pathogenesis of [disease name] is not completely understood. | |||
OR | |||
* It is understood that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3]. | |||
* [Pathogen name] is usually transmitted via the [transmission route] route to the human host. | |||
* Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell. | |||
* [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells]. | |||
* The progression to [disease name] usually involves the [molecular pathway]. | |||
* The pathophysiology of [disease/malignancy] depends on the histological subtype. | |||
== Genetics == | |||
[Disease name] is transmitted in [mode of genetic transmission] pattern. | |||
OR | |||
Genes involved in the pathogenesis of [disease name] include: | |||
* [Gene1] | |||
* [Gene2] | |||
* [Gene3] | |||
OR | |||
The development of [disease name] is the result of multiple genetic mutations such as: | |||
* [Mutation 1] | |||
* [Mutation 2] | |||
* [Mutation 3] | |||
== Associated Conditions == | |||
Conditions associated with [disease name] include: | |||
* [Condition 1] | |||
* [Condition 2] | |||
* [Condition 3] | |||
== Gross Pathology == | |||
On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name]. | |||
== Microscopic Pathology == | |||
On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name]. | |||
== References == | |||
==[[Autoimmune lymphoproliferative syndrome causes|Causes]]== | ==[[Autoimmune lymphoproliferative syndrome causes|Causes]]== | ||
<br /> | |||
== Overview[edit | edit source] == | |||
Disease name] may be caused by [cause1], [cause2], or [cause3]. | |||
OR | |||
Common causes of [disease] include [cause1], [cause2], and [cause3]. | |||
OR | |||
The most common cause of [disease name] is [cause 1]. Less common causes of [disease name] include [cause 2], [cause 3], and [cause 4]. | |||
OR | |||
The cause of [disease name] has not been identified. To review risk factors for the development of [disease name], click here. | |||
== Causes[edit | edit source] == | |||
* ymptom/manifestation] include [cause1], [cause2], and [cause3]. | |||
* [Cause] is a life-threatening cause of [disease]. | |||
=== Common Causes[edit | edit source] === | |||
Common causes of [disease name] may include: | |||
* [Cause1] | |||
* [Cause2] | |||
* [Cause3] | |||
OR | |||
* [Disease name] is caused by an infection with [pathogen name]. | |||
* [Pathogen name] is caused by [pathogen name]. | |||
=== Less Common Causes[edit | edit source] === | |||
Less common causes of [disease name] include: | |||
* [Cause1] | |||
* [Cause2] | |||
* [CauseCauses by OrganList the causes of the disease in alphabetical order: | |||
* Cause 1 | |||
* Cause 2 | |||
* Cause 3 | |||
* Cause 4 | |||
* Cause 5 | |||
* Cause 6 | |||
* Cause 7 | |||
* Cause 8 | |||
* Cause 9 | |||
* Cause 10 | |||
== References == | |||
==[[Autoimmune lymphoproliferative syndrome differential diagnosis|Differentiating Autoimmune lymphoproliferative syndrome from other Diseases]]== | ==[[Autoimmune lymphoproliferative syndrome differential diagnosis|Differentiating Autoimmune lymphoproliferative syndrome from other Diseases]]== | ||
<br /> | |||
== Overview == | |||
[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3]. | |||
OR | |||
[Disease name] must be differentiated from [[differential dx1], [differential dx2], and [differential dx3]. | |||
== Differentiating [Disease name] from other Diseases == | |||
[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3]. | |||
OR | |||
[Disease name] must be differentiated from [differential dx1], [differential dx2], and [differential dx3]. | |||
OR | |||
As [disease name] manifests in a variety of clinical forms, differentiation must be established in accordance with the particular subtype. [Subtype name 1] must be differentiated from other diseases that cause [clinical feature 1], such as [differential dx1] and [differential dx2]. In contrast, [subtype name 2] must be differentiated from other diseases that cause [clinical feature 2], such as [differential dx3] and [differential dx4]. | |||
=== Differentiating [disease name] from other diseases on the basis of [symptom 1], [symptom 2], and [symptom 3] === | |||
On the basis [symptom 1], [symptom 2], and [symptom 3], [disease name] must be differentiated from [disease 1], [disease 2], [disease 3], [disease 4], [disease 5], and [disease 6]. | |||
{| class="wikitable" | |||
! rowspan="4" |Diseases | |||
| colspan="6" rowspan="1" |'''Clinical manifestations''' | |||
! colspan="7" rowspan="2" |Para-clinical findings | |||
| colspan="1" rowspan="4" |'''Gold standard''' | |||
! rowspan="4" |Additional findings | |||
|- | |||
| colspan="3" rowspan="2" |'''Symptoms''' | |||
! colspan="3" rowspan="2" |Physical examination | |||
|- | |||
! colspan="3" |Lab Findings | |||
! colspan="3" |Imaging | |||
! rowspan="2" |Histopathology | |||
|- | |||
!Symptom 1 | |||
! colspan="1" rowspan="1" |Symptom 2 | |||
!Symptom 3 | |||
!Physical exam 1 | |||
! colspan="1" rowspan="1" |Physical exam 2 | |||
!Physical exam 3 | |||
!Lab 1 | |||
!Lab 2 | |||
!Lab 3 | |||
!Imaging 1 | |||
!Imaging 2 | |||
!Imaging 3 | |||
|- | |||
|Differential Diagnosis 1 | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
|- | |||
|Differential Diagnosis 2 | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
|- | |||
|Differential Diagnosis 3 | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
|- | |||
!Diseases | |||
!Symptom 1 | |||
! colspan="1" rowspan="1" |Symptom 2 | |||
!Symptom 3 | |||
!Physical exam 1 | |||
! colspan="1" rowspan="1" |Physical exam 2 | |||
!Physical exam 3 | |||
!Lab 1 | |||
!Lab 2 | |||
!Lab 3 | |||
!Imaging 1 | |||
!Imaging 2 | |||
!Imaging 3 | |||
!Histopathology | |||
|'''Gold standard''' | |||
!Additional findings | |||
|- | |||
|Differential Diagnosis 4 | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
|- | |||
|Differential Diagnosis 5 | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
|- | |||
|Differential Diagnosis 6 | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
| | |||
|} | |||
== References == | |||
==[[Autoimmune lymphoproliferative syndrome epidemiology and demographics|Epidemiology and Demographics]]== | ==[[Autoimmune lymphoproliferative syndrome epidemiology and demographics|Epidemiology and Demographics]]== | ||
== Overview == | |||
== Epidemiology and Demographics == | |||
=== Incidence === | |||
* The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide. | |||
* In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide. | |||
=== Prevalence === | |||
* The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide. | |||
* In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide. | |||
* The prevalence of [disease/malignancy] is estimated to be [number] cases annually. | |||
=== Case-fatality rate/Mortality rate === | |||
* In [year], the incidence of [disease name] is approximately [number range] per 100,000 individuals with a case-fatality rate/mortality rate of [number range]%. | |||
* The case-fatality rate/mortality rate of [disease name] is approximately [number range]. | |||
=== Age === | |||
* Patients of all age groups may develop [disease name]. | |||
* The incidence of [disease name] increases with age; the median age at diagnosis is [#] years. | |||
* [Disease name] commonly affects individuals younger than/older than [number of years] years of age. | |||
* [Chronic disease name] is usually first diagnosed among [age group]. | |||
* [Acute disease name] commonly affects [age group]. | |||
=== Race === | |||
* There is no racial predilection to [disease name]. | |||
* [Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name]. | |||
=== Gender === | |||
* [Disease name] affects men and women equally. | |||
* [Gender 1] are more commonly affected by [disease name] than [gender 2]. The [gender 1] to [gender 2] ratio is approximately [number > 1] to 1. | |||
=== Region === | |||
* The majority of [disease name] cases are reported in [geographical region]. | |||
* [Disease name] is a common/rare disease that tends to affect [patient population 1] and [patient population 2]. | |||
=== Developed Countries === | |||
=== Developing Countries === | |||
== References == | |||
==[[Autoimmune lymphoproliferative syndrome risk factors|Risk Factors]]== | ==[[Autoimmune lymphoproliferative syndrome risk factors|Risk Factors]]== | ||
== Overview == | |||
There are no established risk factors for [disease name]. | |||
OR | |||
The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4]. | |||
OR | |||
Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4]. | |||
OR | |||
Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral. | |||
== Risk Factors == | |||
There are no established risk factors for [disease name]. | |||
OR | |||
The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4]. | |||
OR | |||
Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4]. | |||
=== Common Risk Factors === | |||
* Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral. | |||
* Common risk factors in the development of [disease name] include: | |||
** [Risk factor 1] | |||
** [Risk factor 2] | |||
** [Risk factor 3] | |||
=== Less Common Risk Factors === | |||
* Less common risk factors in the development of [disease name] include: | |||
** [Risk factor 1] | |||
** [Risk factor 2] | |||
** [Risk factor 3] | |||
== References == | |||
==[[Autoimmune lymphoproliferative syndrome screening|Screening]]== | ==[[Autoimmune lymphoproliferative syndrome screening|Screening]]== | ||
== Overview == | |||
There is insufficient evidence to recommend routine screening for [disease/malignancy]. | |||
OR | |||
According to the [guideline name], screening for [disease name] is not recommended. | |||
OR | |||
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3]. | |||
== Screening == | |||
There is insufficient evidence to recommend routine screening for [disease/malignancy]. | |||
OR | |||
According to the [guideline name], screening for [disease name] is not recommended. | |||
OR | |||
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with: | |||
* [Condition 1] | |||
* [Condition 2] | |||
* [Condition 3] | |||
== References == | |||
==[[Autoimmune lymphoproliferative syndrome natural history, complications and prognosis|Natural History, Complications and Prognosis]]== | ==[[Autoimmune lymphoproliferative syndrome natural history, complications and prognosis|Natural History, Complications and Prognosis]]== | ||
== Overview == | |||
If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3]. | |||
OR | |||
Common complications of [disease name] include [complication 1], [complication 2], and [complication 3]. | |||
OR | |||
Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%. | |||
== Natural History, Complications, and Prognosis == | |||
=== Natural History === | |||
* The symptoms of (disease name) usually develop in the first/ second/ third decade of life, and start with symptoms such as ___. | |||
* The symptoms of (disease name) typically develop ___ years after exposure to ___. | |||
* If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3]. | |||
=== Complications === | |||
* Common complications of [disease name] include: | |||
** [Complication 1] | |||
** [Complication 2] | |||
** [Complication 3] | |||
=== Prognosis === | |||
* Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [--]%. | |||
* Depending on the extent of the [tumor/disease progression] at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as poor/good/excellent. | |||
* The presence of [characteristic of disease] is associated with a particularly [good/poor] prognosis among patients with [disease/malignancy]. | |||
* [Subtype of disease/malignancy] is associated with the most favorable prognosis. | |||
* The prognosis varies with the [characteristic] of tumor; [subtype of disease/malignancy] have the most favorable prognosis. | |||
== References == | |||
==Diagnosis== | ==Diagnosis== |
Revision as of 22:13, 21 June 2021
Autoimmune lymphoproliferative syndrome | |
OMIM | 601859 603909 |
---|---|
DiseasesDB | 33425 Template:DiseasesDB2 |
Autoimmune lymphoproliferative syndrome Microchapters |
Differentiating Autoimmune lymphoproliferative syndrome from other Diseases |
---|
Diagnosis |
Treatment |
Case Studies |
Autoimmune lymphoproliferative syndrome On the Web |
American Roentgen Ray Society Images of Autoimmune lymphoproliferative syndrome |
Directions to Hospitals Treating Autoimmune lymphoproliferative syndrome |
Risk calculators and risk factors for Autoimmune lymphoproliferative syndrome |
Editor-In-Chief: David Teachey, MD [1]
Synonyms and keywords: Canale-Smith syndrome; ALPS
Overview
Historical Perspective
Overview[edit | edit source]
Historical Perspective[edit | edit source]
References
Discovery
Overview
The exact pathogenesis of [disease name] is not fully understood.
OR
It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
OR
[Pathogen name] is usually transmitted via the [transmission route] route to the human host.
OR
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
OR
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
OR
The progression to [disease name] usually involves the [molecular pathway].
OR
The pathophysiology of [disease/malignancy] depends on the histological subtype.
Pathophysiology
Physiology
The normal physiology of [name of process] can be understood as follows:
Pathogenesis
- The exact pathogenesis of [disease name] is not completely understood.
OR
- It is understood that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
- [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
- Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
- [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
- The progression to [disease name] usually involves the [molecular pathway].
- The pathophysiology of [disease/malignancy] depends on the histological subtype.
Genetics
[Disease name] is transmitted in [mode of genetic transmission] pattern.
OR
Genes involved in the pathogenesis of [disease name] include:
- [Gene1]
- [Gene2]
- [Gene3]
OR
The development of [disease name] is the result of multiple genetic mutations such as:
- [Mutation 1]
- [Mutation 2]
- [Mutation 3]
Associated Conditions
Conditions associated with [disease name] include:
- [Condition 1]
- [Condition 2]
- [Condition 3]
Gross Pathology
On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Microscopic Pathology
On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
References
Classification
Overview
There is no established system for the classification of [disease name].
OR
[Disease name] may be classified according to [classification method] into [number] subtypes/groups: [group1], [group2], [group3], and [group4].
OR
[Disease name] may be classified into [large number > 6] subtypes based on [classification method 1], [classification method 2], and [classification method 3]. [Disease name] may be classified into several subtypes based on [classification method 1], [classification method 2], and [classification method 3].
OR
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
OR
If the staging system involves specific and characteristic findings and features: According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].
OR
The staging of [malignancy name] is based on the [staging system].
OR
There is no established system for the staging of [malignancy name].
Classification
There is no established system for the classification of [disease name].
OR
[Disease name] may be classified according to [classification method] into [number] subtypes/groups:
- [Group1]
- [Group2]
- [Group3]
- [Group4]
OR
[Disease name] may be classified into [large number > 6] subtypes based on:
- [Classification method 1]
- [Classification method 2]
- [Classification method 3]
[Disease name] may be classified into several subtypes based on:
- [Classification method 1]
- [Classification method 2]
- [Classification method 3]
OR
Based on the duration of symptoms, [disease name] may be classified as either acute or chronic.
OR
If the staging system involves specific and characteristic findings and features:
According to the [staging system + reference], there are [number] stages of [malignancy name] based on the [finding1], [finding2], and [finding3]. Each stage is assigned a [letter/number1] and a [letter/number2] that designate the [feature1] and [feature2].
OR
The staging of [malignancy name] is based on the [staging system].
OR
There is no established system for the staging of [malignancy name].
References
Pathophysiology
Overview
The exact pathogenesis of [disease name] is not fully understood.
OR
It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
OR
[Pathogen name] is usually transmitted via the [transmission route] route to the human host.
OR
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
OR
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
OR
The progression to [disease name] usually involves the [molecular pathway].
OR
The pathophysiology of [disease/malignancy] depends on the histological subtype.
Pathophysiology
Physiology
The normal physiology of [name of process] can be understood as follows:
Pathogenesis
- The exact pathogenesis of [disease name] is not completely understood.
OR
- It is understood that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
- [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
- Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
- [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
- The progression to [disease name] usually involves the [molecular pathway].
- The pathophysiology of [disease/malignancy] depends on the histological subtype.
Genetics
[Disease name] is transmitted in [mode of genetic transmission] pattern.
OR
Genes involved in the pathogenesis of [disease name] include:
- [Gene1]
- [Gene2]
- [Gene3]
OR
The development of [disease name] is the result of multiple genetic mutations such as:
- [Mutation 1]
- [Mutation 2]
- [Mutation 3]
Associated Conditions
Conditions associated with [disease name] include:
- [Condition 1]
- [Condition 2]
- [Condition 3]
Gross Pathology
On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Microscopic Pathology
On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
References
Causes
Overview[edit | edit source]
Disease name] may be caused by [cause1], [cause2], or [cause3].
OR
Common causes of [disease] include [cause1], [cause2], and [cause3].
OR
The most common cause of [disease name] is [cause 1]. Less common causes of [disease name] include [cause 2], [cause 3], and [cause 4].
OR
The cause of [disease name] has not been identified. To review risk factors for the development of [disease name], click here.
Causes[edit | edit source]
- ymptom/manifestation] include [cause1], [cause2], and [cause3].
- [Cause] is a life-threatening cause of [disease].
Common Causes[edit | edit source]
Common causes of [disease name] may include:
- [Cause1]
- [Cause2]
- [Cause3]
OR
- [Disease name] is caused by an infection with [pathogen name].
- [Pathogen name] is caused by [pathogen name].
Less Common Causes[edit | edit source]
Less common causes of [disease name] include:
- [Cause1]
- [Cause2]
- [CauseCauses by OrganList the causes of the disease in alphabetical order:
- Cause 1
- Cause 2
- Cause 3
- Cause 4
- Cause 5
- Cause 6
- Cause 7
- Cause 8
- Cause 9
- Cause 10
References
Differentiating Autoimmune lymphoproliferative syndrome from other Diseases
Overview
[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].
OR
[Disease name] must be differentiated from [[differential dx1], [differential dx2], and [differential dx3].
Differentiating [Disease name] from other Diseases
[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].
OR
[Disease name] must be differentiated from [differential dx1], [differential dx2], and [differential dx3].
OR
As [disease name] manifests in a variety of clinical forms, differentiation must be established in accordance with the particular subtype. [Subtype name 1] must be differentiated from other diseases that cause [clinical feature 1], such as [differential dx1] and [differential dx2]. In contrast, [subtype name 2] must be differentiated from other diseases that cause [clinical feature 2], such as [differential dx3] and [differential dx4].
Differentiating [disease name] from other diseases on the basis of [symptom 1], [symptom 2], and [symptom 3]
On the basis [symptom 1], [symptom 2], and [symptom 3], [disease name] must be differentiated from [disease 1], [disease 2], [disease 3], [disease 4], [disease 5], and [disease 6].
Diseases | Clinical manifestations | Para-clinical findings | Gold standard | Additional findings | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Symptoms | Physical examination | ||||||||||||||
Lab Findings | Imaging | Histopathology | |||||||||||||
Symptom 1 | Symptom 2 | Symptom 3 | Physical exam 1 | Physical exam 2 | Physical exam 3 | Lab 1 | Lab 2 | Lab 3 | Imaging 1 | Imaging 2 | Imaging 3 | ||||
Differential Diagnosis 1 | |||||||||||||||
Differential Diagnosis 2 | |||||||||||||||
Differential Diagnosis 3 | |||||||||||||||
Diseases | Symptom 1 | Symptom 2 | Symptom 3 | Physical exam 1 | Physical exam 2 | Physical exam 3 | Lab 1 | Lab 2 | Lab 3 | Imaging 1 | Imaging 2 | Imaging 3 | Histopathology | Gold standard | Additional findings |
Differential Diagnosis 4 | |||||||||||||||
Differential Diagnosis 5 | |||||||||||||||
Differential Diagnosis 6 |
References
Epidemiology and Demographics
Overview
Epidemiology and Demographics
Incidence
- The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
- In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.
Prevalence
- The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
- In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.
- The prevalence of [disease/malignancy] is estimated to be [number] cases annually.
Case-fatality rate/Mortality rate
- In [year], the incidence of [disease name] is approximately [number range] per 100,000 individuals with a case-fatality rate/mortality rate of [number range]%.
- The case-fatality rate/mortality rate of [disease name] is approximately [number range].
Age
- Patients of all age groups may develop [disease name].
- The incidence of [disease name] increases with age; the median age at diagnosis is [#] years.
- [Disease name] commonly affects individuals younger than/older than [number of years] years of age.
- [Chronic disease name] is usually first diagnosed among [age group].
- [Acute disease name] commonly affects [age group].
Race
- There is no racial predilection to [disease name].
- [Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].
Gender
- [Disease name] affects men and women equally.
- [Gender 1] are more commonly affected by [disease name] than [gender 2]. The [gender 1] to [gender 2] ratio is approximately [number > 1] to 1.
Region
- The majority of [disease name] cases are reported in [geographical region].
- [Disease name] is a common/rare disease that tends to affect [patient population 1] and [patient population 2].
Developed Countries
Developing Countries
References
Risk Factors
Overview
There are no established risk factors for [disease name].
OR
The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
OR
Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
OR
Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
Risk Factors
There are no established risk factors for [disease name].
OR
The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
OR
Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
Common Risk Factors
- Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
- Common risk factors in the development of [disease name] include:
- [Risk factor 1]
- [Risk factor 2]
- [Risk factor 3]
Less Common Risk Factors
- Less common risk factors in the development of [disease name] include:
- [Risk factor 1]
- [Risk factor 2]
- [Risk factor 3]
References
Screening
Overview
There is insufficient evidence to recommend routine screening for [disease/malignancy].
OR
According to the [guideline name], screening for [disease name] is not recommended.
OR
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3].
Screening
There is insufficient evidence to recommend routine screening for [disease/malignancy].
OR
According to the [guideline name], screening for [disease name] is not recommended.
OR
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with:
- [Condition 1]
- [Condition 2]
- [Condition 3]
References
Natural History, Complications and Prognosis
Overview
If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
OR
Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
OR
Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.
Natural History, Complications, and Prognosis
Natural History
- The symptoms of (disease name) usually develop in the first/ second/ third decade of life, and start with symptoms such as ___.
- The symptoms of (disease name) typically develop ___ years after exposure to ___.
- If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
Complications
- Common complications of [disease name] include:
- [Complication 1]
- [Complication 2]
- [Complication 3]
Prognosis
- Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [--]%.
- Depending on the extent of the [tumor/disease progression] at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as poor/good/excellent.
- The presence of [characteristic of disease] is associated with a particularly [good/poor] prognosis among patients with [disease/malignancy].
- [Subtype of disease/malignancy] is associated with the most favorable prognosis.
- The prognosis varies with the [characteristic] of tumor; [subtype of disease/malignancy] have the most favorable prognosis.
References
Diagnosis
Diagnostic Criteria | History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | Chest X Ray | CT | MRI | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies