Malignant Angioendotheliomatosis Is an Angiotropic Intravascular Lymphoma
Autor: | M. S. Daoud, W. P. D. Su, R. K. Winkelmann, Charles Perniciaro |
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Rok vydání: | 1995 |
Předmět: |
Male
Pathology medicine.medical_specialty Lymphoma B-Cell Skin Neoplasms Dermatology Fibrin Pathology and Forensic Medicine Angioma Biopsy medicine Humans Lymphocytes Molecular Biology Aged Aged 80 and over Gene Rearrangement Genes Immunoglobulin biology medicine.diagnostic_test business.industry Vascular disease Lymphoma Non-Hodgkin General Medicine Middle Aged medicine.disease Lymphoma Microscopy Electron Phenotype medicine.anatomical_structure biology.protein Blood Vessels Immunohistochemistry Female Panniculitis business Blood vessel |
Zdroj: | The American Journal of Dermatopathology. 17:242-248 |
ISSN: | 0193-1091 |
DOI: | 10.1097/00000372-199506000-00005 |
Popis: | Malignant angioendotheliomatosis is a rare intravascular (angiotropic) lymphoma. Patients most often present with cutaneous or central nervous system findings. We describe three patients with malignant angioendotheliomatosis involving the skin. The initial lesions in each were tender, indurated nodules on the lower extremities, resembling inflammatory panniculitis. Skin biopsies and immunohistochemical studies from all patients confirmed intravascular B-cell lymphoma. Two patients had visceral involvement, and molecular genetics studies showed clonal immunoglobulin gene rearrangement in one. Electron microscopy in this case showed increased fibrin and atypical lymphocytes within blood vessels. Malignant angioendotheliomatosis is a monoclonal intravascular lymphoma, usually of B-cell phenotype. Occlusion of small blood vessels with lymphoid cells, fibrin, and degenerating cellular debris causes the cutaneous lesions. An excisional biopsy through the depth of subcutaneous tissue may be necessary to confirm the diagnosis of malignant angioendotheliomatosis. |
Databáze: | OpenAIRE |
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