Appendix cancer differential diagnosis: Difference between revisions
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| colspan="2" style="background: #DCDCDC; padding: 5px;" |[[Pseudomyxoma peritonei differential diagnosis|Pseudomyxoma peritonei]] | | colspan="2" style="background: #DCDCDC; padding: 5px;" |[[Pseudomyxoma peritonei differential diagnosis|Pseudomyxoma peritonei]] | ||
|<nowiki>+</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>+</nowiki> | ||
|<nowiki>+</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>+</nowiki> | ||
| +/-Diarrhea | | style="background: #F5F5F5; padding: 5px;" |+/-Diarrhea | ||
<nowiki>+/-</nowiki>Constipation | <nowiki>+/-</nowiki>Constipation | ||
|Bloating | |style="background: #F5F5F5; padding: 5px;" |Bloating | ||
|<nowiki>-</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>-</nowiki> | ||
|<nowiki>+</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>+</nowiki> | ||
|[[Ascites]] | |style="background: #F5F5F5; padding: 5px;" |[[Ascites]] | ||
Shifting dullness | Shifting dullness | ||
|<nowiki>-</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>-</nowiki> | ||
| | |style="background: #F5F5F5; padding: 5px;" | | ||
* Non specific | * Non specific | ||
* Depends on the etiology of the disease | * Depends on the etiology of the disease | ||
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* Low-attenuation | * Low-attenuation | ||
* Scalloping of the visceral surfaces differentiates pseudomyxoma from other causes of peritnoitis. | * Scalloping of the visceral surfaces differentiates pseudomyxoma from other causes of peritnoitis. | ||
* Typically does not invade visceral organs or spread by [[lymphatic]] or hematogenous routes unlike mucinous carcinomatosis | * Typically does not invade visceral organs or spread by [[lymphatic]] or hematogenous routes unlike mucinous carcinomatosis | ||
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Characterized by a mass which is hypointense on T1-weighted MRI and hyperintense on T2-weighted MRI. MRI has better sensitivity in detecting ascites fluid and mucocele. | Characterized by a mass which is hypointense on T1-weighted MRI and hyperintense on T2-weighted MRI. MRI has better sensitivity in detecting ascites fluid and mucocele. | ||
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* The echoes within pseudomyxoma peritonei are not mobile. | * The echoes within pseudomyxoma peritonei are not mobile. | ||
* Echogenic septations within the gelatinous ascites. | * Echogenic septations within the gelatinous ascites. | ||
* Scalloping of the [[hepatic]] and splenic margins | * Scalloping of the [[hepatic]] and splenic margins | ||
|18F-FDG [[PET scan]] | |18F-FDG [[PET scan]] | ||
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* Depending on [[WHO]]<nowiki/>classification, whether it's low or high grade with cellular atypia or acellular mucin. ( DPAM, PMCA) | * Depending on [[WHO]]<nowiki/>classification, whether it's low or high grade with cellular atypia or acellular mucin. ( DPAM, PMCA) | ||
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*:* [[MUC2]] | *:* [[MUC2]] | ||
*:* MUC5AC | *:* MUC5AC | ||
| | |style="background: #F5F5F5; padding: 5px;" | | ||
* Diagnostic laparascopy/laparatomy | * Diagnostic laparascopy/laparatomy | ||
|- | |- | ||
| colspan="2" style="background: #DCDCDC; padding: 5px;" |[[Carcinoid syndrome]] | | colspan="2" style="background: #DCDCDC; padding: 5px;" |[[Carcinoid syndrome]] | ||
|<nowiki>-/+</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>-/+</nowiki> | ||
|<nowiki>-</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>-</nowiki> | ||
|Diarrhea | |style="background: #F5F5F5; padding: 5px;" |Diarrhea | ||
|Flushing | |style="background: #F5F5F5; padding: 5px;" |Flushing | ||
Palpitation | Palpitation | ||
Dyspnea | Dyspnea | ||
|<nowiki>-</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>-</nowiki> | ||
|<nowiki>-</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>-</nowiki> | ||
| | |style="background: #F5F5F5; padding: 5px;" | | ||
* Tricuspid regurgitation | * Tricuspid regurgitation | ||
* murmur | * murmur | ||
* Wheezing | * Wheezing | ||
|<nowiki>+</nowiki> | |style="background: #F5F5F5; padding: 5px;" |<nowiki>+</nowiki> | ||
|Depends on the tumor [[Neuroendocrine tumors laboratory findings|type]]: | |style="background: #F5F5F5; padding: 5px;" |Depends on the tumor [[Neuroendocrine tumors laboratory findings|type]]: | ||
* Ki67 | * Ki67 | ||
* N-terminal pro–B-type natriuretic peptide | * N-terminal pro–B-type natriuretic peptide | ||
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* [[Pancreatic polypeptide]] | * [[Pancreatic polypeptide]] | ||
* | * | ||
|Depends on the primary tumor location and type | |style="background: #F5F5F5; padding: 5px;" |Depends on the primary tumor location and type | ||
|Depends on the primary tumor location and type | |style="background: #F5F5F5; padding: 5px;" |Depends on the primary tumor location and type | ||
|Depends on the primary tumor location and type | |style="background: #F5F5F5; padding: 5px;" |Depends on the primary tumor location and type | ||
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* [[Somatostatin]] [[scintigraphy]] with 111-indium-octreotide | * [[Somatostatin]] [[scintigraphy]] with 111-indium-octreotide | ||
* [[Bone]] [[scintigraphy]] with 99mTc-methylene diphosphonate (99mTcMDP) | * [[Bone]] [[scintigraphy]] with 99mTc-methylene diphosphonate (99mTcMDP) | ||
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* [[Endoscopic]] [[ultrasonography]] (EUS) | * [[Endoscopic]] [[ultrasonography]] (EUS) | ||
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* Salt and pepper nuclei | * Salt and pepper nuclei | ||
* Cellular uniformity | * Cellular uniformity | ||
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** CD56 and PGP ( less specific) | ** CD56 and PGP ( less specific) | ||
** PDX1 and ISL1 | ** PDX1 and ISL1 | ||
|[[Biopsy]] from the tumor is the gold standard method of diagnosis, meanwhile | |style="background: #F5F5F5; padding: 5px;" |[[Biopsy]] from the tumor is the gold standard method of diagnosis, meanwhile | ||
5-HIAA (5-hydroxyindoleacetic acid) is the most specific marker of carcinoid tumors | 5-HIAA (5-hydroxyindoleacetic acid) is the most specific marker of carcinoid tumors |
Revision as of 19:35, 12 February 2019
Appendix cancer Microchapters |
Diagnosis |
---|
Treatment |
Appendix cancer differential diagnosis On the Web |
American Roentgen Ray Society Images of Appendix cancer differential diagnosis |
Risk calculators and risk factors for Appendix cancer differential diagnosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Soroush Seifirad, M.D.[2]
Overview
appendix cancer 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
appendix cancer must be differentiated from [[differential dx1], [differential dx2], and [differential dx3].
Differentiating appendix cancer from other Diseases
appendix cancer 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
appendix cancer must be differentiated from [differential dx1], [differential dx2], and [differential dx3].
OR
As appendix cancer 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 appendix cancer from other diseases on the basis of [symptom 1], [symptom 2], and [symptom 3]
On the basis [symptom 1], [symptom 2], and [symptom 3], appendix cancer 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 | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Symptoms | Physical examination | |||||||||||||||
Lab Findings | Imaging | Histopathology | ||||||||||||||
Abdominal pain | Change in girdle size | Change in bowel habits | Other symptoms | Abdominal mass | abdominal tenderness | Other physical examination findings | Urinary 5-hydroxyindoleacetic acid (5-HIAA) and/or Serum Chromogranin A (CgA) | Other lab findings | CT scan | MRI | Utrasounography | Other diagnostic studies and imaging modalities | ||||
Appendix cancer | Adenocarcinoma1 | +/- | -/+ | Constipation |
|
- | - |
|
- |
|
|
|
|
Positron emission tomography (PET) | Gross pathology:
Microscopic pathology:???????????????????????????? |
Biopsy |
Carcinoid tumor2 | +/- | - | Diarrhea |
|
- | - |
|
+ |
|
|
Gross pathology:
Microscopic pathology:??????????????? |
Biopsy | ||||
Goblet cell carcinoid | ||||||||||||||||
Lymphoma | ||||||||||||||||
Appendix Mucocele | Mucosal hyperlasia | - | - | - |
|
- | +/- | N/A | - | N/A |
|
|Rounded right iliac fossa mass
|
|
N/A | Similar to hyperplastic colon polyp | Biopsy |
Simple or retention cyst | - | - | - | - | +/- | - | - | N/A | Degenerative epithelial changes because of obstruction | Biopsy | ||||||
Mucinous cystadenomas | +/- | +/- | +/-Diarrhea
+/-Constipation |
|
+/- | +/- | If develop pseudomyxoma peritonei:
|
- |
|
|
Biopsy | |||||
Mucinous cystadenocarcinomas | +/- | +/- | +/-Diarrhea
+/-Constipation |
+/- | +/- | - | - |
|
|
Biopsy | ||||||
Ovarian cancer | +/- | +/- | +/-Constipation |
|
+ | +/- |
|
- |
|
|
|
|
N/A | Depends on the tumor type. You may find the details here. | Biopsy | |
Colorectal cancer | +/- | +/- | +/-Diarrhea
+ Constipation |
|
+ | +/- | ??????? | -/+(Carcinoid tumors) |
|
luminal narrowing, intestinal wall thickening,intussusception, bowel obstruction, hepatic metastases, intestinal perforation,enlarged lymph nodes |
|
Generally not recommended: may evaluate liver metastasis or presence of fluid in abdominal cavity, but it is neither sensitive nor specific. | PET scan, Endoscopy, Colonoscopy,
Barium enema |
|
Biopsy | |
Pseudomyxoma peritonei | + | + | +/-Diarrhea
+/-Constipation |
Bloating | - | + | Ascites
Shifting dullness |
- |
|
|
Characterized by a mass which is hypointense on T1-weighted MRI and hyperintense on T2-weighted MRI. MRI has better sensitivity in detecting ascites fluid and mucocele. |
|
18F-FDG PET scan |
|
| |
Carcinoid syndrome | -/+ | - | Diarrhea | Flushing
Palpitation Dyspnea |
- | - |
|
+ | Depends on the tumor type:
|
Depends on the primary tumor location and type | Depends on the primary tumor location and type | Depends on the primary tumor location and type |
|
|
Biopsy from the tumor is the gold standard method of diagnosis, meanwhile
5-HIAA (5-hydroxyindoleacetic acid) is the most specific marker of carcinoid tumors | |
Appendicitis 3 | LLQ / RRQ | - | +/- Diarrhea
+ Constipation |
Nausea & vomiting,decreased appetite
Anorexia |
+/- | + |
|
- |
|
Appendiceal wall thickening /perforation
peri-appendiceal inflammation, fluid accumulation,fat stranding |
Increased fluid signal on T2 weighted sequence | Evidences of inflammation
|
Tc-99m labeled anti-CD15 antibodies | Evidences of inflammation | A combination of Imaging (ultrasonography or CT scan, while CT scan is more sensitive), physical exam and history |
1 Adenocarcinomas usually present with appendicitis, barely they might present with Pseudomyxoma peritonei; meanwhile Pseudomyxoma peritonei is more prevalent in perforated mucocele, goblet cell tumor or high stages of adenocarcinoma.
2 Generally appendix carcinoids are asymptomatic, they were only become symptomatic if they metastasize to the liver, or in rare cases make an obstruction and present with appendicitis which is quit uncommon in appendiceal carcinoids compared to appendiceal adenocarcinoma. Any patient with carcinoid syndrome should be evaluated for appendix carcinoids.
3 Every patient with appendicitis should be evaluated for appendix cancer, 0.5 in 100 appendicitis cases are because of appendix cancer.