Results 71 to 80 of about 1,421,260 (161)

Glomeruloid hemangioma in normal individuals

Indian Journal of Dermatology, 2013
Glomeruloid hemangioma is a rare, histologically distinctive, cutaneous, benign vascular tumor, originally described by Chan et al. Glomeruloid hemangioma appears specific to polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin ...
Jyoti Gupta, Rajat Kandhari, V Ramesh, Avninder Singh   +3 more
doaj   +1 more source

Endocrine Manifestations in POEMS Syndrome: a case report and literature review

BMC Endocrine Disorders, 2019
Background POEMS syndrome, a rare systemic disease, is characterized by 5 components: Peripheral neuropathy, Organomegaly, Endocrinopathy, M protein elevation, and Skin changes.
Hui Li, Yumeng Huang, Yan Li, Baozhong Zheng, Jingqiu Cui, Ming Liu   +5 more
doaj   +1 more source

POEMS Syndrome

, 2020
Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes (POEMS) syndrome is a rare disorder due to an underlying plasma cell clone (PC). The syndrome can affect several organs.
Meulemans, N, Doyen, Chantal, Depaus, Julien   +2 more
core  

POEMS syndrome with undetectable M-protein: a case report and literature review

Diagnostic Pathology
Background Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome is a rare plasma cell (PC) neoplasm with associated paraneoplastic syndrome. According to the current diagnostic criteria, peripheral polyneuropathy and
Han-Yue Xue, Lin Zhou, Qin-Zhao Yuan, Yang Zhang, Yi-Qun Hao, Shao-Wei Chen, Hong-Kun Wang, Fang Wei   +7 more
doaj   +1 more source

Castleman disease of the hyaline vascular variant transforming to POEMS syndrome as endpoint: a case report

BMC Neurology, 2018
Background POEMS syndrome is a rare neoplastic syndrome reflected by plasma cell disorder. It is composed by polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes. It is also reported to associate with Castleman disease.
Yijun Ge, Qian Da, Ying Dai
doaj   +1 more source

Case series on POEMS Syndrome- a rare paraneoplastic disorder [PDF]

POEMS syndrome, also known as Crow-Fukase syndrome or Takatsuki syndrome, is a rare paraneoplastic disorder linked to an underlying plasma cell neoplasm.
Dr Shubham Satyanarayan Agrawal; Dr Ramji Sharma; Dr Rahul Gupta; Dr Mayank Gupta
core   +1 more source

Case report: Atypical POEMS syndrome without polyneuropathy, complicated by borderline TAFRO syndrome

Frontiers in Medicine
POEMS syndrome is a complex and rare hematological disease involving multiple physiological systems. According to the currently accepted diagnostic criteria for POEMS syndrome, polyneuropathy is one of the primary mandatory criteria.
Shuai Tan, Mingyue Shang, Yasufumi Masaki, Jing Ni, Yuwei Da, Jing Sun, Yaofang Cao, Li Su, Wanling Sun   +8 more
doaj   +1 more source

Syndrome POEMS et papilloedème.

, 1992
The Crow-Fukase syndrome or POEMS syndrome (Polyneuropathy, Organomegaly, Edema, Monoclonal protein, Skin changes) is an uncommon plasma cell dyscrasia leading to a multisystemic disorder. An optic disc swelling is often related to this syndrome.
Schakal, Alexandre, Cordonnier, Monique, Soupart, Alain   +2 more
core  

Poems Syndrome (osteosclerotic Myeloma) [síndrome De Poems (mieloma Osteoesclerótico)]

, 2015
POEMS syndrome is a unique clinical entity defined by the presence of a monoclonal plasma cell disorder, peripheral neuropathy, and other paraneoplastic features such as organomegaly, endocrinopathy, skin changes, papilledema, sclerotic bone lesions ...
Pinto Neto J.V.
core   +1 more source

A case report of an M protein-negative patient with POEMS syndrome associated with renal involvement

BMC Nephrology
Background POEMS syndrome with polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes is an uncommon plasma cell paraneoplastic syndrome involving multiple system.
Wenlin Liu, Yue Zhou, Lingyan Li, Fan Zhang, Zuying Xiong, Shuang Hou   +5 more
doaj   +1 more source