Results 71 to 80 of about 3,468 (180)

Unusual Neurological Manifestation of Langerhans Cell Histiocytosis in an Adult

Ear, Nose & Throat Journal
Langerhans Cell Histiocytosis is a rare disorder characterized by an abnormal proliferation of Langerhans cells in one or multiple organs. It rarely presents with a central vestibular involvement.
Imen Achour MD, Ines Kharrat MD, Youssef Hbaieb MD, Mariam Ben Ayed MD, Malek Mnejja MD, Bouthaina Hammami MD, Basma Souissi MD, Ilhem Charfeddine MD   +7 more
doaj   +1 more source

Langerhans cell histiocytosis in sphenoid sinus with vision impairment: Case report and literature review

Science Progress
Langerhans cell histiocytosis (LCH) is a neoplastic disease characterized by aberrant proliferation of the mononuclear phagocyte system, predominantly affecting children under the age of 3 years.
Min-Shan Li, Xing-Liang Wu, Ao Huang, Heng Wang   +3 more
doaj   +1 more source

Sinus Histiocytosis [PDF]

, 2020
openaire   +1 more source

Mesothelial cell inclusions mimicking adenocarcinoma in cervical lymph nodes in association with chylous effusion

Indian Journal of Medical and Paediatric Oncology, 2010
Mesothelial cell inclusions in lymph nodes are of rare occurrence and can be mistaken as metastatic adenocarcinomas, mesothelioma or sinus histiocytosis.
Goyal Manu, Kodandapani Suseela, Sharanabasappa S, Palanki Satya   +3 more
doaj  

Rosai–Dorfman Disease of Nasal Soft Tissue: A Case Report

Ear, Nose & Throat Journal
Rosai–Dorfman disease (RDD) is characterized by sinus histiocytosis with massive lymphadenopathy, and the tissue exhibits positive results for S100 and CD68. This lesion typically affects the lymph nodes and rarely involves the nasal soft tissues.
Liwen Wang BS, Huicheng Gong MM, Linlan Jiang MM, Shuyi Gao BS, Yuenong Jiao BS   +4 more
doaj   +1 more source

Rosai-Dorfman disease presenting with extensive cutaneous manifestation - Case report Doença de Rosai-Dorfman com manifestação cutânea extensa - Relato de caso

Anais Brasileiros de Dermatologia, 2013
Rosai-Dorfman disease is a benign, self-limited, idiopathic proliferative histiocytic disorder. It was first described in 1969 by Rosai and Dorfman. In its typical form the disease is characterized by extensive cervical lymphadenopathy associated with ...
Paula Azevedo Borges Leal, Adrilena Lopes Adriano, Marcelle Parente Breckenfeld, Igor Santos Costa, Antônio Renê Diógenes de Sousa, Heitor de Sá Gonçalves   +5 more
doaj  

Spindle Cell (Metaplastic) Carcinoma of the Breast Showing No Clinical Benefit with Pembrolizumab-Based Neoadjuvant Chemoimmunotherapy. [PDF]

Surg Case Rep
Yamada R, Kai K, Hidaka K, Yoshii D, Shirotani R, Takahashi T, Miyasato Y, Murakami S, Mikami Y, Komohara Y, Yamamoto Y.   +10 more
europepmc   +1 more source

Rosai-Dorfman disease presenting as isolated cervical lymphadenopathy in a young adult: A case report. [PDF]

Radiol Case Rep
Rguyeg A, Boutahar M, Lachkar A.
europepmc   +1 more source

Primary Cutaneous Rosai-Dorfman Disease With Typical Immunophenotype But Lacking Emperipolesis: A Case Report. [PDF]

Clin Med Insights Case Rep
Al-Soufi L, Marashli A, Younis R, Alkasem AS, Hussein F, Al-Shehabi Z.   +5 more
europepmc   +1 more source

Nasal Rosai-Dorfman disease: A case report and review of the literature. [PDF]

SAGE Open Med Case Rep
Yang J, Yang G.
europepmc   +1 more source