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Immunoproliferative Disorder Information

Immunoproliferative disorders (also known as “immunoproliferative diseases” or “immunoproliferative neoplasms”) are disorders of the immune system that are characterized by the abnormal proliferation of the primary cells of the immune system, which includes B cells, T cells and Natural killer (NK) cells, or by the excessive production of immunoglobulins (also known as antibodies).

Contents

Classes

These disorders are subdivided into three main classes, which are lymphoproliferative disorders, hypergammaglobulinemia, and paraproteinemia.[1] The first is cellular, and the other two are humoral (however, humoral excess can be secondary to cellular excess.)

See also

References

  1. ^ Health Communication Network. Immunoproliferative disorders - Topic Tree. http://www.use.hcn.com.au/subject.%60Immunoproliferative%20Disorders%60/home.html. Accessed March 2007.

External links

Pathology: Medical conditions and ICD code
(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)
(A/B, 001–139) Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease (Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis
(C/D, 140–239 & 279–289)
Cancer (C00–D48, 140–239) Tumor
Myeloid hematologic (D50–D77, 280–289) Anemia · Coagulopathy
Lymphoid immune (D80–D89, 279) Immunodeficiency · Immunoproliferative disorder · Hypersensitivity
(E, 240–278) Endocrine disease · Nutrition disorder · Inborn error of metabolism
(F, 290–319) Mental disorder
(G, 320–359) Nervous system disease (CNS, PNS) · Neuromuscular disease
(H, 360–389) Eye disease · Ear disease
(I, 390–459) Cardiovascular disease (Heart disease, Vascular disease)
(J, 460–519) Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia)
(K, 520–579) Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach, Enteropathy, Liver, Pancreatic)
(L, 680–709) Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)
(M, 710–739) Musculoskeletal disorders: Myopathy · Arthropathy · Osteochondropathy (Osteopathy, Chondropathy)
(N, 580–629) Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast disease · Female genital disease
(O, 630–679) Complications of pregnancy · Obstetric labor complication · Puerperal disorder
(P, 760–779) Fetal disease
(Q, 740–759) Congenital disorder (Congenital abnormality)
(R, 780–799) Syndromes · Medical signs (Eponymous)
(S/T, 800–999) Bone fracture · Joint dislocation · Sprain · Strain · Subluxation · Head injury · Chest trauma · Poisoning
Immune disorders, Immunoproliferative immunoglobulin disorders (D89, 273)
PCDs/PP Plasmacytoma · Multiple myeloma (Plasma cell leukemia) · MGUS · IgM (Macroglobulinemia/Waldenström's macroglobulinemia) · heavy chain (Heavy chain disease) · light chain (Primary amyloidosis)
Other hypergammaglobulinemia Cryoglobulinemia

: LMC

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Hematological malignancy/leukemia histology (ICD-O 9590–9989, C81–C96, 200–208) Lymphoid/Lymphoproliferative, Lymphomas/Lymphoid leukemias (9590–9739, 9800–9839)
B cell (lymphoma, leukemia) (most CD19, CD20)
By development/ marker
TdT+ ALL (Precursor B acute lymphoblastic leukemia/lymphoma)
CD5+ naive B cell (CLL/SLL) mantle zone (Mantle cell)
CD22+ Prolymphocytic · CD11c (Hairy cell leukemia)
CD79a+ germinal center/follicular B cell (Follicular, Burkitt's, GCB-DLBCL) marginal zone/marginal-zone B cell (Splenic marginal zone, MALT, Nodal marginal zone)
RS (CD15+, CD30+) Classic Hodgkin's lymphoma (Nodular sclerosis) · CD20 (Nodular lymphocyte predominant Hodgkin's lymphoma)
PCDs/PP (CD38+/CD138+) see
By infection KSHV (Primary effusion) · EBV (Lymphomatoid granulomatosis, Post-transplant lymphoproliferative disorder) · HIV (AIDS-related lymphoma) · Helicobacter pylori (MALT lymphoma)
Ungrouped Diffuse large B-cell lymphomaIntravascular large B-cell lymphomaPrimary cutaneous marginal zone lymphomaPrimary cutaneous immunocytomaPlasmacytomaPlasmacytosis
T/NK
T cell (lymphoma, leukemia) (most CD3, CD4, CD8)
By development/ marker

TdT+: ALL (Precursor T acute lymphoblastic leukemia/lymphoma)

prolymphocyte (Prolymphocytic)

CD30+ (Anaplastic large cell, Lymphomatoid papulosis)
By location/peripheral Cutaneous (Mycosis fungoides, Sézary's disease) · Hepatosplenic · Angioimmunoblastic · Enteropathy-associated T-cell lymphoma
By infection HTLV-1 (Adult T-cell leukemia/lymphoma)
NK cell/ (most CD56) Aggressive NK-cell leukemia · Blastic NK cell lymphoma
T or NK EBV (Extranodal NK-T-cell lymphoma) · Large granular lymphocytic leukemia
Ungrouped CD30+ cutaneous T-cell lymphomaAngioimmunoblastic T-cell lymphomaSubcutaneous T-cell lymphomaNon-mycosis fungoides CD30− cutaneous large T-cell lymphomaPleomorphic T-cell lymphomaLennert lymphomaSecondary cutaneous CD30+ large cell lymphomaAngiocentric lymphoma
Lymphoid+myeloid Acute biphenotypic leukaemia
Lymphocytosis Lymphoproliferative disorders (X-linked lymphoproliferative disease, Autoimmune lymphoproliferative syndrome) · Leukemoid reaction · Pseudolymphoma · Diffuse infiltrative lymphocytosis syndrome
Ungrouped lymphoid-related cutaneous conditions Cutaneous lymphoid hyperplasiaCutaneous lymphoid hyperplasia with bandlike and perivascular patternsCutaneous lymphoid hyperplasia with nodular patternJessner lymphocytic infiltrate of the skin Granulomatous slack skinKikuchi diseaseLeukemia cutisLymphomatoid papulosisLeukemidPagetoid reticulosisPrimary cutaneous follicular lymphomaSinus histiocytosis with massive lymphadenopathy

: LMC

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Categories: Immune system disorders

 

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