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Malignant angioendotheliomatosis mimicking systemic necrotizing vasculitis.
J Rheumatol. 1992 Jul; 19(7):1133-5.JR

Abstract

Malignant angioendotheliomatosis is a rare disease characterized by an intravascular proliferation of atypical mononuclear cells. Manifestations result from occlusion of small blood vessels. Multiple organ systems are involved and the clinical presentation resembles a systemic necrotizing vasculitis with skin and central nervous system most commonly involved. The clinical course is characterized by progressive organ failure with death usually within 2 years after presentation. Based on its assumed origin as an intravascular lymphoma, patients may respond to chemotherapy.

Authors+Show Affiliations

Lutheran General Hospital, Division of Medicine, Park Ridge, IL 60068.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

1512773

Citation

Kao, N L., et al. "Malignant Angioendotheliomatosis Mimicking Systemic Necrotizing Vasculitis." The Journal of Rheumatology, vol. 19, no. 7, 1992, pp. 1133-5.
Kao NL, Broy S, Tillawi I. Malignant angioendotheliomatosis mimicking systemic necrotizing vasculitis. J Rheumatol. 1992;19(7):1133-5.
Kao, N. L., Broy, S., & Tillawi, I. (1992). Malignant angioendotheliomatosis mimicking systemic necrotizing vasculitis. The Journal of Rheumatology, 19(7), 1133-5.
Kao NL, Broy S, Tillawi I. Malignant Angioendotheliomatosis Mimicking Systemic Necrotizing Vasculitis. J Rheumatol. 1992;19(7):1133-5. PubMed PMID: 1512773.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Malignant angioendotheliomatosis mimicking systemic necrotizing vasculitis. AU - Kao,N L, AU - Broy,S, AU - Tillawi,I, PY - 1992/7/1/pubmed PY - 1992/7/1/medline PY - 1992/7/1/entrez SP - 1133 EP - 5 JF - The Journal of rheumatology JO - J Rheumatol VL - 19 IS - 7 N2 - Malignant angioendotheliomatosis is a rare disease characterized by an intravascular proliferation of atypical mononuclear cells. Manifestations result from occlusion of small blood vessels. Multiple organ systems are involved and the clinical presentation resembles a systemic necrotizing vasculitis with skin and central nervous system most commonly involved. The clinical course is characterized by progressive organ failure with death usually within 2 years after presentation. Based on its assumed origin as an intravascular lymphoma, patients may respond to chemotherapy. SN - 0315-162X UR - https://www.unboundmedicine.com/medline/citation/1512773/Malignant_angioendotheliomatosis_mimicking_systemic_necrotizing_vasculitis_ L2 - http://www.diseaseinfosearch.org/result/9633 DB - PRIME DP - Unbound Medicine ER -
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