Primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report
Primary skin amyloidosis is a chronic skin disease in which amyloid deposits in the normal skin tissues without involving other organs. At present, the causes and mechanisms of morbidity have not been fully elucidated. There are few clinical reports of nodular skin amyloidosis, and the domestic repo...
Guardado en:
Autores principales: | , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
De Gruyter
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/b316062d2aec42479198f5ad5478339f |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:b316062d2aec42479198f5ad5478339f |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:b316062d2aec42479198f5ad5478339f2021-12-05T14:10:41ZPrimary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report2391-541210.1515/biol-2021-0076https://doaj.org/article/b316062d2aec42479198f5ad5478339f2021-08-01T00:00:00Zhttps://doi.org/10.1515/biol-2021-0076https://doaj.org/toc/2391-5412Primary skin amyloidosis is a chronic skin disease in which amyloid deposits in the normal skin tissues without involving other organs. At present, the causes and mechanisms of morbidity have not been fully elucidated. There are few clinical reports of nodular skin amyloidosis, and the domestic reports are mostly limited cases. This study reported a rare case of a 46-year-old woman with primary localized cutaneous nodular amyloidosis (PLCNA). The patient presented with features of lymphatic malformation, a plexiform nodule of small blisters. Histological examination revealed amyloid deposits involving the superficial and deep dermis with a small number of plasma cells. Further examinations did not reveal evidence of systemic involvement, indicating a PLCNA. The presentation as lymphatic malformation lesions illustrates the importance of clinical pathology. Nodular amyloidosis typically manifests as single or multiple yellow-brown nodules or plaques of a few millimeters to several centimeters. The center of the nodule sometimes shows atrophy and relaxation or forms a bullous. It is recommended to perform a pathological examination to confirm the diagnosis to distinguish it from lymphatic malformation.Wu XiujuanZhao ZongfengDe Gruyterarticlenodular amyloidosislymphatic malformationBiology (General)QH301-705.5ENOpen Life Sciences, Vol 16, Iss 1, Pp 781-784 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
nodular amyloidosis lymphatic malformation Biology (General) QH301-705.5 |
spellingShingle |
nodular amyloidosis lymphatic malformation Biology (General) QH301-705.5 Wu Xiujuan Zhao Zongfeng Primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report |
description |
Primary skin amyloidosis is a chronic skin disease in which amyloid deposits in the normal skin tissues without involving other organs. At present, the causes and mechanisms of morbidity have not been fully elucidated. There are few clinical reports of nodular skin amyloidosis, and the domestic reports are mostly limited cases. This study reported a rare case of a 46-year-old woman with primary localized cutaneous nodular amyloidosis (PLCNA). The patient presented with features of lymphatic malformation, a plexiform nodule of small blisters. Histological examination revealed amyloid deposits involving the superficial and deep dermis with a small number of plasma cells. Further examinations did not reveal evidence of systemic involvement, indicating a PLCNA. The presentation as lymphatic malformation lesions illustrates the importance of clinical pathology. Nodular amyloidosis typically manifests as single or multiple yellow-brown nodules or plaques of a few millimeters to several centimeters. The center of the nodule sometimes shows atrophy and relaxation or forms a bullous. It is recommended to perform a pathological examination to confirm the diagnosis to distinguish it from lymphatic malformation. |
format |
article |
author |
Wu Xiujuan Zhao Zongfeng |
author_facet |
Wu Xiujuan Zhao Zongfeng |
author_sort |
Wu Xiujuan |
title |
Primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report |
title_short |
Primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report |
title_full |
Primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report |
title_fullStr |
Primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report |
title_full_unstemmed |
Primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: A case report |
title_sort |
primary localized cutaneous nodular amyloidosis presenting as lymphatic malformation: a case report |
publisher |
De Gruyter |
publishDate |
2021 |
url |
https://doaj.org/article/b316062d2aec42479198f5ad5478339f |
work_keys_str_mv |
AT wuxiujuan primarylocalizedcutaneousnodularamyloidosispresentingaslymphaticmalformationacasereport AT zhaozongfeng primarylocalizedcutaneousnodularamyloidosispresentingaslymphaticmalformationacasereport |
_version_ |
1718371860170670080 |