Lymphadenopathy causes: Difference between revisions

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| '''Hematologic'''
| '''Hematologic'''
|bgcolor="Beige"| [[Acute lymphoblastic leukemia]], [[Acute lymphocytic leukemia]], [[Adult T cell leukemia]], [[Autoimmune lymphoproliferative syndrome type 1]], [[Castleman's disease]], [[Chronic lymphocytic leukemia]], [[Cutaneous T cell lymphoma]],[[Familial hemophagocytic lymphohistiocytosis]], [[Familial histiocytic reticulosis]], [[Faisalabad histiocytosis]], [[Gamma heavy chain disease]], [[Hairy cell leukaemia]], [[Hemoblastosis]], [[Hemophagocytic reticulosis]], [[Histiocytosis X]],[[Hodgkin's Lymphoma]], [[Hyperimmunoglobulinemia D and periodic fever syndrome]], [[Large granular lymphocyte leukemia]],[[Leukemia]], [[Lipogranulomatosis]], [[Lymphangioma]], [[Lymphoma]], [[Macroglobulinemia]], [[Myeloproliferative disorder]],[[Non-Hodgkin's Lymphoma]], [[Primary autoimmune haemolytic anaemia]], [[Plasma cell leukemia]], [[Reticuloendotheliosis]],[[Sinus histiocytosis]], [[Systemic mastocytosis]], [[Waldenström macroglobulinaemia]], [[X-linked agammaglobulinaemia]],[[X-linked lymphoproliferative syndrome]], [[WT limb blood syndrome]]
|bgcolor="Beige"| [[Acute lymphoblastic leukemia]], [[Acute lymphocytic leukemia]], [[Adult T cell leukemia]], [[Autoimmune lymphoproliferative syndrome type 1]], [[Castleman's disease]], [[Chronic lymphocytic leukemia]], [[Cutaneous T cell lymphoma]],[[Familial hemophagocytic lymphohistiocytosis]], [[Familial histiocytic reticulosis]], [[Faisalabad histiocytosis]], [[Gamma heavy chain disease]], [[Hairy cell leukaemia]], [[Hemoblastosis]], [[Hemophagocytic reticulosis]], [[Histiocytosis X]],[[Hodgkin's Lymphoma]], [[Hyperimmunoglobulinemia D and periodic fever syndrome]], [[Large granular lymphocyte leukemia]],[[Leukemia]], [[Lipogranulomatosis]], [[Lymphangioma]], [[Lymphoma]], [[Macroglobulinemia]], [[Myeloproliferative disorder]],[[Non-Hodgkin's Lymphoma]], [[Primary autoimmune haemolytic anaemia]], [[Plasma cell leukemia]], [[Reticuloendotheliosis]],[[Sinus histiocytosis]], [[Systemic mastocytosis]], [[Waldenström macroglobulinemia]], [[X-linked agammaglobulinaemia]],[[X-linked lymphoproliferative syndrome]], [[WT limb blood syndrome]]
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*[[Visceral leishmaniasis]] / [[Kala-azar]]
*[[Visceral leishmaniasis]] / [[Kala-azar]]


*[[Waldenström macroglobulinaemia]]
*[[Waldenström macroglobulinemia]]


*[[Western equine encephalitis]]
*[[Western equine encephalitis]]
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*[[Extrinsic allergic alveolitis]]
*[[Extrinsic allergic alveolitis]]
*[[Pneumoconiosis]]
*[[Pneumoconiosis]]


==References==
==References==

Revision as of 22:24, 30 July 2012

Lymphadenopathy Microchapters

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Differentiating Lymphadenopathy from other Diseases

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]

Overview

Causes

Common Causes

Causes by Organ System

Cardiovascular No underlying causes
Chemical / poisoning No underlying causes
Dermatologic Erythroderma, Infantile papular acrodermatitis, Melanoma, Merkel cell carcinoma, Mycosis fungoides
Drug Side Effect Allopurinol, Atenolol , Captopril, Carbamazepine , Cephalosporins, Gold,Hydralazine, Penicillin, Phenytoin, Phenytoin, Primidone, Pyrimethamine, Quinidine, Sulfonamides,Sulindac, Yaws
Ear Nose Throat No underlying causes
Endocrine Hyperthyroidism
Environmental No underlying causes
Gastroenterologic Hepatitis A, Hepatitis B, Mesenteric adenitis, Stomach cancer, Tang Hsi Ryu syndrome,Whipple's disease
Genetic Familial alphalipoprotein deficiency, Familial hemophagocytic lymphohistiocytosis, Familial histiocytic reticulosis, X-linked agammaglobulinaemia, X-linked lymphoproliferative syndrome
Hematologic Acute lymphoblastic leukemia, Acute lymphocytic leukemia, Adult T cell leukemia, Autoimmune lymphoproliferative syndrome type 1, Castleman's disease, Chronic lymphocytic leukemia, Cutaneous T cell lymphoma,Familial hemophagocytic lymphohistiocytosis, Familial histiocytic reticulosis, Faisalabad histiocytosis, Gamma heavy chain disease, Hairy cell leukaemia, Hemoblastosis, Hemophagocytic reticulosis, Histiocytosis X,Hodgkin's Lymphoma, Hyperimmunoglobulinemia D and periodic fever syndrome, Large granular lymphocyte leukemia,Leukemia, Lipogranulomatosis, Lymphangioma, Lymphoma, Macroglobulinemia, Myeloproliferative disorder,Non-Hodgkin's Lymphoma, Primary autoimmune haemolytic anaemia, Plasma cell leukemia, Reticuloendotheliosis,Sinus histiocytosis, Systemic mastocytosis, Waldenström macroglobulinemia, X-linked agammaglobulinaemia,X-linked lymphoproliferative syndrome, WT limb blood syndrome
Iatrogenic No underlying causes
Infectious Disease Bacteria:

Anthrax, Borrelia burgdorferi, Bortonneuse fever, Brucellosis, Cat scratch disease, Congenital tuberculosis, Erysipelas, Granuloma inguinale, Lepromatous leprosy, Listeriosis, Lymphogranuloma venereum,Mastitis, Moraxella catarrhalis, Mycobacterium avium-intracellulare, Mycobacterium chelonei, Pinta,Plague, Rat-bite fever, Rickettsiae, Scrub typhus, Sennetsu fever, Septicaemia, Spotted fevers,Streptococcal tonsillitis, Syphilis, Three-day fever, Tuberculosis, Tularemia, Typhus fever, Vincent's angina, Yersinia pestis

Virus:

AIDS, Cowpox, Coxsackie virus, Cytomegalovirus infection, Dengue, German Measles/Rubella, Hepatitis A, Hepatitis B, Herpes simplex, Infectious mononucleosis, Influenza, Lassa fever, Measles, Mumps,Smallpox, Varicella, Western equine encephalitis

Fungal:

Coccidioidomycosis, Blastomycosis, Histoplasmosis, Sporotrichosis

Parasitic:

African Sleeping sickness, Chagas' disease, Congenital Toxoplasmosis, Filaria, Lymphatic filariasis,Onchocerciasis, Opisthorchiasis, Paracoccidioidomycosis, Rhabditida Infections, Toxoplasmosis,Trypanosomiasis, Visceral leishmaniasis /Kala-azar, Wuchereria bancrofti

Musculoskeletal / Ortho Juvenile chronic arthritis, WT limb blood syndrome
Neurologic Tang Hsi Ryu syndrome
Nutritional / Metabolic Apo A-I deficiency, Sphingomyelinase deficiency
Obstetric/Gynecologic No underlying causes
Oncologic Acute lymphoblastic leukemia, Acute lymphocytic leukemia, Adult T cell leukemia, Breast cancer, Colorectal cancer, Chronic lymphocytic leukemia, Hemangiopericytoma, Lip cancer, Malignant lymphoma, Melanoma, Metastasis, Non-Hodgkin's Lymphoma, Pancoast tumor, Pseudolymphoma,Rhabdomyosarcoma, Stomach cancer, Cutaneous T cell lymphoma, Hairy cell leukaemia, Hodgkin's Lymphoma,Large granular lymphocyte leukemia, Lymphoma, Plasma cell leukemia, Merkel cell carcinoma, Mycosis fungoides,WT limb blood syndrome
Opthalmologic No underlying causes
Overdose / Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary Extrinsic allergic alveolitis, Pneumoconiosis, Sarcoidosis
Renal / Electrolyte No underlying causes
Rheum / Immune / Allergy Angioimmunoblastic lymphadenopathy, Angioimmunoblastic with dysproteinemia lymphadenopathy,Autoimmune lymphoproliferative syndrome type 1, Caspase-8 deficiency, Chediak-Higashi syndrome, Churg-Strauss syndrome, Common Variable Immunodeficiency, Extrinsic allergic alveolitis, Griscelli disease, Primary autoimmune haemolytic anaemia, Rheumatoid arthritis, Serum sickness, Siccardi syndrome, Still's Disease, Systemic lupus erythematosus/SLE, Sarcoidosis
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Dental No underlying causes
Miscellaneous Amyloidosis, Aphthous stomatitis, Bejel, Black widow spider envenomation, Cystic hygroma,Gingivostomatitis, Idiopathic, Radiotherapy, Snake bite (Viperidae), Spider bite, Vaccination

Causes in Alphabetical Order[3] [4]


Bihilar lymphadenopathy

The causes can divide into the four commonest:

Less common causes include:

References

  1. ↑ 1.0 1.1 Status and anamnesis, Anders Albinsson. Page 12
  2. ↑ Chris Jennings (1993). "Understanding and Preventing AIDS: A Book for Everyone".
  3. ↑ Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:77 ISBN 1591032016
  4. ↑ Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:68 ISBN 140510368X
  5. ↑ Blum JA, Neumayr AL, Hatz CF (2012). "Human African trypanosomiasis in endemic populations and travellers". Eur. J. Clin. Microbiol. Infect. Dis. 31 (6): 905–13. doi:10.1007/s10096-011-1403-y. PMID 21901632. Unknown parameter |month= ignored (help)
  6. ↑ Beukes CA, Thiart J (2012). "The incidence of human herpes virus-8 expression in lymph node biopsies from human immunodeficiency virus-positive patients". Histopathology. doi:10.1111/j.1365-2559.2012.04291.x. PMID 22716315. Unknown parameter |month= ignored (help)
  7. ↑ Mitsuhashi K, Shiseki M, Ishiyama M; et al. (2011). "[Angioimmunoblastic T-cell lymphoma with marked polyclonal plasmacytosis in peripheral blood and bone marrow mimicking plasma cell leukemia]". Rinsho Ketsueki (in Japanese). 52 (7): 563–9. PMID 21821991. Unknown parameter |month= ignored (help)
  8. ↑ Simonelli S, Gianazza E, Mombelli G; et al. (2012). "Severe high-density lipoprotein deficiency associated with autoantibodies against lecithin:cholesterol acyltransferase in non-Hodgkin lymphoma". Arch. Intern. Med. 172 (2): 179–81. doi:10.1001/archinternmed.2011.661. PMID 22271127. Unknown parameter |month= ignored (help)
  9. ↑ Simesen de Bielke MG, Yancoski J, Rocco C; et al. (2012). "A Missense Mutation in the Extracellular Domain of Fas: The Most Common Change in Argentinean Patients with Autoimmune Lymphoproliferative Syndrome Represents a Founder Effect". J Clin Immunol. doi:10.1007/s10875-012-9731-y. PMID 22752343. Unknown parameter |month= ignored (help)
  10. ↑ Schleenvoigt BT, Keller P, Stallmach A, Pletz MW (2012). "[African tick bite fever--rickettsiosis after holiday in South Africa]". Dtsch. Med. Wochenschr. (in German). 137 (17): 891–3. doi:10.1055/s-0032-1304902. PMID 22511280. Unknown parameter |month= ignored (help)
  11. ↑ Roushan MR, Amiri MJ (2012). "Update on Childhood Brucellosis". Recent Pat Antiinfect Drug Discov. PMID 22812616. Unknown parameter |month= ignored (help)
  12. ↑ Dispenzieri A, Armitage JO, Loe MJ; et al. (2012). "The clinical spectrum of Castleman's disease". Am J Hematol. doi:10.1002/ajh.23291. PMID 22791417. Unknown parameter |month= ignored (help)
  13. ↑ Chondrogiannis K, Vezakis A, Derpapas M, Melemeni A, Fragulidis G (2012). "Seronegative cat-scratch disease diagnosed by PCR detection of Bartonella henselae DNA in lymph node samples". Braz J Infect Dis. 16 (1): 96–9. PMID 22358366.
  14. ↑ 14.0 14.1 Reddy RR, Babu BM, Venkateshwaramma B, Hymavathi Ch (2011). "Silvery hair syndrome in two cousins: Chediak-Higashi syndrome vs Griscelli syndrome, with rare associations". Int J Trichology. 3 (2): 107–11. doi:10.4103/0974-7753.90825. PMC 3250006. PMID 22223973. Unknown parameter |month= ignored (help)
  15. ↑ Fantinato GT, Cestari Sda C, Afonso JP, Sousa LS, Enokihara MM (2011). "Do you know this syndrome? Chediak-Higashi syndrome". An Bras Dermatol. 86 (5): 1029. PMID 22147054.
  16. ↑ Warnatz K, Voll RE (2012). "Pathogenesis of autoimmunity in common variable immunodeficiency". Front Immunol. 3: 210. doi:10.3389/fimmu.2012.00210. PMC 3399211. PMID 22826712.
  17. ↑ 17.0 17.1 Goyal T, Varshney A (2012). "A rare presentation of erythrodermic mycosis fungoides". Cutis. 89 (5): 229–32, 236. PMID 22768436. Unknown parameter |month= ignored (help)
  18. ↑ information at the Histiocytosis Association of America
  19. ↑ Bieliauskas S, Tubbs RR, Bacon CM; et al. (2012). "Gamma heavy-chain disease: defining the spectrum of associated lymphoproliferative disorders through analysis of 13 cases". Am. J. Surg. Pathol. 36 (4): 534–43. doi:10.1097/PAS.0b013e318240590a. PMID 22301495. Unknown parameter |month= ignored (help)



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