Immunoblastic lymphadenopathy with purpura and cryoglobulinemia

Wechsler, H. L.

doi:10.1001/archderm.113.5.636

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Laboratory Findings In Aild1

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1995

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Cited by 6 publications

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“…Polyclonal hypergammaglobulinemia is the most common protein abnormality in AILD, occurring in 75 % of cases [33], but early or late hypogammaglobulinemia [9,19,52,73,76,85], IgA deficiency [13,86], monoclonal gammopathies [l, 17,75,76], cryoglobulinemia [6,10,13], cryofibrinogenemia [4], and cold agglutinins [4,13,33] have all been reported.…”

Section: Laboratory Findings In Aildmentioning

confidence: 99%

Angioimmunoblastic lymphadenopathy

Azevedo

Yunis

1985

American J Hematol

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Section: Laboratory Findings In Aildmentioning

confidence: 99%

Angioimmunoblastic lymphadenopathy

Azevedo

Yunis

1985

American J Hematol

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Pulmonary Polymorphic Centroblastic Type Malignant Lymphoma in a Patient with Lymphomatoid Granulomatosis, Sjögren Syndrome and Other Manifestations of a Dysimmune State

Capron

Audouin

Diébold

et al. 1985

Pathology - Research and Practice

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Skin lesions in angioimmunoblastic lymphadenopathy: histological and immunological studies

Bernengo

Levi²,

Zina

1981

Br J Dermatol

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Angioimmunoblastic lymphadenopathy with drysproteinaemia is reported (AILD) in four patients with different skin pictures. As the disease progresses two main forms predominate; papulonodular and erythroderma. In all cases the histological picture of the skin mirrors that of the lymph-node. Our results point to an increase in the peripheral blood, lymph-nodes and skin of T and subsequently of B lymphocytes suggesting that a proliferation of helper T cells and hence activation of the B-cell subpopulation may be involved in the pathogenesis of some cases of AILD.

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Immunoblastic lymphadenopathy with purpura and cryoglobulinemia

Cited by 6 publications

References 0 publications

Angioimmunoblastic lymphadenopathy

Angioimmunoblastic lymphadenopathy

Pulmonary Polymorphic Centroblastic Type Malignant Lymphoma in a Patient with Lymphomatoid Granulomatosis, Sjögren Syndrome and Other Manifestations of a Dysimmune State

Skin lesions in angioimmunoblastic lymphadenopathy: histological and immunological studies

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