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[Systemic proliferative angioendotheliomatosis: a cutaneous manifestation of malignant B-cell lymphomas. Histologic and immunohistologic studies of two cases].
Hautarzt 1991; 42(6):384-90H

Abstract

Angioendotheliomatosis proliferans systemisata (AEPS) is a rare disease entity characterized by a predominantly intravascular proliferation of tumour cells. Two forms of AEPS are differentiated: a very rare, benign and self-limiting form, which is endothelial in origin, and a more common, malignant form, which is an angiotropic intravascular malignant B-cell lymphoma. Histological and immunohistological investigations of the malignant form of AEPS are presented: In a 69-year-old woman cutaneous lesions appeared 5 months before the diagnosis of B-immunoblastic lymphoma. In a 57-year-old woman lesions were observed simultaneously with the relapse of a high-grade malignant B-cell lymphoma. Immunohistological identification of the proliferating cell type made diagnosis of intravascular B-cell lymphoma possible in paraffin-embedded biopsies.

Authors+Show Affiliations

Dermatohistologisches Labor der Gemeinschaftspraxis, Friedrichshafen.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

ger

PubMed ID

1917462

Citation

Kutzner, H, et al. "[Systemic Proliferative Angioendotheliomatosis: a Cutaneous Manifestation of Malignant B-cell Lymphomas. Histologic and Immunohistologic Studies of Two Cases]." Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete, vol. 42, no. 6, 1991, pp. 384-90.
Kutzner H, Englert W, Hellenbroich D, et al. [Systemic proliferative angioendotheliomatosis: a cutaneous manifestation of malignant B-cell lymphomas. Histologic and immunohistologic studies of two cases]. Hautarzt. 1991;42(6):384-90.
Kutzner, H., Englert, W., Hellenbroich, D., Embacher, G., Kutzner, U., & Schröder, J. (1991). [Systemic proliferative angioendotheliomatosis: a cutaneous manifestation of malignant B-cell lymphomas. Histologic and immunohistologic studies of two cases]. Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete, 42(6), pp. 384-90.
Kutzner H, et al. [Systemic Proliferative Angioendotheliomatosis: a Cutaneous Manifestation of Malignant B-cell Lymphomas. Histologic and Immunohistologic Studies of Two Cases]. Hautarzt. 1991;42(6):384-90. PubMed PMID: 1917462.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Systemic proliferative angioendotheliomatosis: a cutaneous manifestation of malignant B-cell lymphomas. Histologic and immunohistologic studies of two cases]. AU - Kutzner,H, AU - Englert,W, AU - Hellenbroich,D, AU - Embacher,G, AU - Kutzner,U, AU - Schröder,J, PY - 1991/6/1/pubmed PY - 1991/6/1/medline PY - 1991/6/1/entrez SP - 384 EP - 90 JF - Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete JO - Hautarzt VL - 42 IS - 6 N2 - Angioendotheliomatosis proliferans systemisata (AEPS) is a rare disease entity characterized by a predominantly intravascular proliferation of tumour cells. Two forms of AEPS are differentiated: a very rare, benign and self-limiting form, which is endothelial in origin, and a more common, malignant form, which is an angiotropic intravascular malignant B-cell lymphoma. Histological and immunohistological investigations of the malignant form of AEPS are presented: In a 69-year-old woman cutaneous lesions appeared 5 months before the diagnosis of B-immunoblastic lymphoma. In a 57-year-old woman lesions were observed simultaneously with the relapse of a high-grade malignant B-cell lymphoma. Immunohistological identification of the proliferating cell type made diagnosis of intravascular B-cell lymphoma possible in paraffin-embedded biopsies. SN - 0017-8470 UR - https://www.unboundmedicine.com/medline/citation/1917462/[Systemic_proliferative_angioendotheliomatosis:_a_cutaneous_manifestation_of_malignant_B_cell_lymphomas__Histologic_and_immunohistologic_studies_of_two_cases]_ L2 - http://www.diseaseinfosearch.org/result/2041 DB - PRIME DP - Unbound Medicine ER -