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Paraneoplastic autoimmune multiorgan syndrome (paraneoplastic pemphigus) with unusual manifestations and without detectable autoantibodies.
Indian J Dermatol Venereol Leprol ; 2014 Jul-Aug; 80(4): 328-330
Article in English | IMSEAR | ID: sea-154852
ABSTRACT
We describe a patient with paraneoplastic autoimmune multiorgan syndrome (PAMS) secondary to a lymphoblastic T‑ cell lymphoma who presented with a lichenoid dermatitis and vitiligo, later developing bronchiolitis obliterans and autoimmune hepatitis. Notably, he had no detectable autoantibodies. The development of vitiligo and autoimmune hepatic involvement probably indicate a role for cytotoxic T‑ cell lymphocytes in the pathogenesis of this syndrome.

Full text: Available Index: IMSEAR (South-East Asia) Language: English Journal: Indian J Dermatol Venereol Leprol Year: 2014 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Language: English Journal: Indian J Dermatol Venereol Leprol Year: 2014 Type: Article