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[Plasmocytoma-associated bullous hemorrhagic amyloidosis of the skin].
Hautarzt. 1982 Oct; 33(10):556-8.H

Abstract

Case report of a 70-year-old woman with plasmocytoma-associated bullous "amyloid purpura" and a lambda light-chain IgA paraproteinemia. Cutaneous hemorrhage with blisters, erosions, and milia in the intertriginous areas were the main clinical features. Amyloid deposits in the walls of blood vessels, and the pericollagenous affinity of the amyloid in the dermis are likely to be responsible for the increased capillary fragility, i.e., the hemorrhagic tendency and the infrapapillary blisters. A differentiation from epidermolysis bullosa acquisita and porphyria cutanea tarda is possible by means of the histological level of the blisters.

Authors

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Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

ger

PubMed ID

6759462

Citation

Hödl, S, et al. "[Plasmocytoma-associated Bullous Hemorrhagic Amyloidosis of the Skin]." Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete, vol. 33, no. 10, 1982, pp. 556-8.
Hödl S, Turek TD, Kerl H. [Plasmocytoma-associated bullous hemorrhagic amyloidosis of the skin]. Hautarzt. 1982;33(10):556-8.
Hödl, S., Turek, T. D., & Kerl, H. (1982). [Plasmocytoma-associated bullous hemorrhagic amyloidosis of the skin]. Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete, 33(10), 556-8.
Hödl S, Turek TD, Kerl H. [Plasmocytoma-associated Bullous Hemorrhagic Amyloidosis of the Skin]. Hautarzt. 1982;33(10):556-8. PubMed PMID: 6759462.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Plasmocytoma-associated bullous hemorrhagic amyloidosis of the skin]. AU - Hödl,S, AU - Turek,T D, AU - Kerl,H, PY - 1982/10/1/pubmed PY - 1982/10/1/medline PY - 1982/10/1/entrez SP - 556 EP - 8 JF - Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete JO - Hautarzt VL - 33 IS - 10 N2 - Case report of a 70-year-old woman with plasmocytoma-associated bullous "amyloid purpura" and a lambda light-chain IgA paraproteinemia. Cutaneous hemorrhage with blisters, erosions, and milia in the intertriginous areas were the main clinical features. Amyloid deposits in the walls of blood vessels, and the pericollagenous affinity of the amyloid in the dermis are likely to be responsible for the increased capillary fragility, i.e., the hemorrhagic tendency and the infrapapillary blisters. A differentiation from epidermolysis bullosa acquisita and porphyria cutanea tarda is possible by means of the histological level of the blisters. SN - 0017-8470 UR - https://www.unboundmedicine.com/medline/citation/6759462/[Plasmocytoma_associated_bullous_hemorrhagic_amyloidosis_of_the_skin]_ L2 - http://www.diseaseinfosearch.org/result/380 DB - PRIME DP - Unbound Medicine ER -
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