Zobrazeno 1 - 10
of 121
pro vyhledávání: '"non-langerhans histiocytosis"'
Autor:
Feryal El Oualladi, MD, Mohamed Labied, MD, Rabab Hassani, MD, Chorouk Mountassir, MD, Ghizlane Lembarki, MD, Mouna Sabiri, PhD, Samira Lezar, PhD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 5619-5623 (2024)
Erdheim-Chester disease (ECD) is a rare form of non-Langerhans cell histiocytosis. There are few documented cases in the medical literature. Here, we present an infrequent case of a 53-year-old patient who presented with cutaneous xanthelasma and a g
Externí odkaz:
https://doaj.org/article/487c521341044d2f861332b2cb69b596
Akademický článek
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Autor:
Andrea RodrÃguez Trigueros, José Ramón Lopez-Morales, José Carlos Alarcón GarcÃa, Santiago RodrÃguez Suárez, Pilar Sancho, José Salvador GarcÃa-Morillo
Publikováno v:
Spanish Journal of Medicine, Vol 2, Iss 4 (2022)
Erdheim-Chester disease (ECD) is a non-Langerhans histiocytic that typically affects middle-aged adults between the fifth and seventh decades of life. It is characterized by systemic xanthogranulomatous infiltration by histiocytes CD68+/CD1a–. In t
Externí odkaz:
https://doaj.org/article/aa752bf9e99e4f3e82d6d5e1d0100aae
Publikováno v:
Case Reports in Dermatology, Vol 13, Iss 2, Pp 399-406 (2021)
Juvenile xanthogranuloma (JXG) is the most common type of non-Langerhans cell histiocytosis. JXG is a rare benign tumor, which may be present at birth or develop later. The classical form of JXG is characterized by a red-yellowish benign papule or no
Externí odkaz:
https://doaj.org/article/4635241875db4592b72a85fdf15acd66
Autor:
Joshua Makary, Prem Rathore
Publikováno v:
Urology Case Reports, Vol 43, Iss , Pp 102062- (2022)
In this report we describe the clinical journey of a 62-year-old male that presented with acute kidney injury secondary to Erdheim-Chester disease, a non-Langerhans variant of histiocytosis rarely encountered by urological surgeons. ECD can uncommonl
Externí odkaz:
https://doaj.org/article/5c0ff72c7d1e489a88f93784bb9d2c6d
Publikováno v:
Indian Spine Journal, Vol 4, Iss 1, Pp 133-137 (2021)
Erdheim–Chester disease (ECD) is a rare non-Langerhans histiocytosis. Appendicular skeleton involvement is more common whereas axial skeletal manifestation is very rare. Isolated thoracic spine involvement with myelopathy in ECD is reported extreme
Externí odkaz:
https://doaj.org/article/317dcd4ae3d84b1d8c29868ba5d9f43b
Bone mineral density and bone microarchitecture in a cohort of patients with Erdheim-Chester Disease
Autor:
Tianhua He, Lijia Cui, Na Niu, Fengdan Wang, Huilei Miao, Hao Zhao, Xuemin Gao, Chang Liu, Fan Yu, Yan Jiang, Ou Wang, Mei Li, Xiaoping Xing, Daobin Zhou, Jian Li, Xinxin Cao, Weibo Xia
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Erdheim-Chester Disease (ECD) is a rare type of non-Langerhans histiocytosis. Skeletal structures are affected in over 95% ECD patients. Due to the lack of proper imaging assessment tools, the alteration of bone microarchitecture
Externí odkaz:
https://doaj.org/article/f5c5a5c9f1ce400d9df1ee2aaa51e1de
Publikováno v:
Dermatologica Sinica, Vol 38, Iss 3, Pp 176-179 (2020)
The non-Langerhans cell histiocytoses (non-LCH) are rare and benign histiocytic disorders. We present a 61-year-old female with progressive skin-colored nodules on the face and extremities. The skin biopsy showed dermal infiltration of foamy histiocy
Externí odkaz:
https://doaj.org/article/b49bc1619dcd4c3f9acb787ddd10e165
Publikováno v:
Indian Journal of Ophthalmology, Vol 68, Iss 9, Pp 2054-2056 (2020)
An immunocompetent, 25-year-old gentleman with bilateral chronic uveitis presented to various uveitis clinics at different points of time with documented typical clinical features of Toxoplasma Chorioretinitis (Headlight in fog appearance), Behcet's
Externí odkaz:
https://doaj.org/article/38ed34918a1049939900e4fa4c9038c3
Publikováno v:
Case Reports in Ophthalmology, Vol 9, Iss 1, Pp 76-81 (2018)
Background: Necrobiotic xanthogranuloma (NXG) is a rare non-Langerhans histiocytosis with cutaneous manifestations, most commonly of the periorbital skin, and is often associated with hematologic disorders such as monoclonal gammopathy. Treatment of
Externí odkaz:
https://doaj.org/article/cb12132b35204a059c5ecb5a1726c242