Results 51 to 60 of about 6,881 (266)

Diagnostic Importance of Cutaneous Manifestations of Neurofibromatosis—A Systematic Review

Neurology and Clinical Neuroscience, Volume 13, Issue 3, Page 165-173, May 2025.
ABSTRACT A class of hereditary diseases known as neurofibromatoses results in tumor growth on tissue from nerves. The spinal cord, nerves, and brain are among the parts of the nervous framework where these tumors can form. Similar to other genetic disorders, neurofibromatosis discloses complicated phenotypes, exhibiting varying benign and malignant ...
Hina Aslam, Inshal Jawed, Ali Farhan, Vikash Karmani, Agha Muhammad Wali Mirza, Farah Alam, Hina Khan, Abdul Haseeb, Mohammad Omer Alam, Javed Iqbal, Brijesh Sathian, Abu Huraira Bin Gulzar   +11 more
wiley   +1 more source

BRAF V600E mutation in Juvenile Xanthogranuloma family neoplasms of the central nervous system (CNS-JXG): a revised diagnostic algorithm to include pediatric Erdheim-Chester disease

Acta Neuropathologica Communications, 2019
The family of juvenile xanthogranuloma family neoplasms (JXG) with ERK-pathway mutations are now classified within the “L” (Langerhans) group, which includes Langerhans cell histiocytosis (LCH) and Erdheim Chester disease (ECD).
J. Picarsic, T. Pysher, Holly Zhou, M. Fluchel, T. Pettit, M. Whitehead, Lea F. Surrey, B. Harding, G. Goldstein, Y. Fellig, M. Weintraub, B. Mobley, P. Sharples, M. Sulis, E. Diamond, R. Jaffe, K. Shekdar, M. Santi   +17 more
semanticscholar   +1 more source

Adult-Onset Asthma with Periocular Xanthogranuloma (AAPOX), a Variant of Periorbital Xanthogranulomatous Disease: An Uncommon Entity

Indian Dermatology Online Journal, 2020
Adult orbital xanthogranulomatous disease (AOXGD) is a rare granulomatous disorder. Adult-onset asthma with periocular xanthogranuloma (AAPOX) which is a subtype of AOXGD is very rare and a realtively unknown entity among dermatologists.
Kananbala Sahu, Madhusmita Sethy, C. Sirka, A. Rout   +3 more
semanticscholar   +1 more source

The various clinical spectra of juvenile xanthogranuloma: imaging for two case reports and review of the literature

BMC Pediatrics, 2019
BackgroundJuvenile xanthogranuloma (JXG) belongs to the heterogeneous group of non-Langerhans cell histiocytosis and is caused by an accumulation and proliferation of macrophages.
Michael Höck, B. Zelger, Gisela Schweigmann, B. Brunner, B. Zelger, G. Kropshofer, U. Kiechl-Kohlendorfer   +6 more
semanticscholar   +1 more source

Hepatic Xanthogranuloma that Originated from a Liver Cyst and Mimicked a Malignant Tumor

In Vivo, 2020
Background/Aim: Hepatic xanthogranuloma is a very rale disease and formation process is unknown. Case Report: A 69-year-old woman previously diagnosed as simple liver cyst. Two years before, a 36-mm liver cyst was found in segment 5, while one year later,
Eri Oda, T. Beppu, K. Kinoshita, K. Yamamura, N. Sato, H. Yuki, Suguru Chiyonaga, T. Motohara, Yoshihiko Komohara, S. Akahoshi   +9 more
semanticscholar   +1 more source

Juvenile Xanthogranuloma Presenting as Bilateral Non-Infiltrative Extraconal Superior Orbital Tumour in a 27 Year Old Nigerian Woman: Features, Management and Outcome

Clinical Medicine Insights: Case Reports, 2012
Introduction Orbital masses in adults are often caused by systemic diseases or are associated with systemic manifestations. Juvenile xanthogranuloma as a cause is rare and unreported in Africa.
Okosa Michael Chuka, Anyiam Daniel Chukwuemeka Darlinton   +1 more
doaj   +1 more source

Multiple generalized xanthogranuloma in adult: Case report and treatment

Indian Journal of Dermatology, 2011
Xanthogranuloma is a benign, asymptomatic, and self-healing disorder of non-Langerhans cell histiocytosis, affecting mostly infants, children, and rarely adults. Diagnosis is easy in typical cases but become more complex in unusual forms.
Arun Achar, Biswanath Naskar, Prabodh Chandra Mondal, Mallika Pal   +3 more
doaj   +1 more source

Upper eyelid juvenile xanthogranuloma: a case report

Revista Brasileira de Oftalmologia, 2021
Juvenile xanthogranuloma is a rare benign non-Langerhans cell histiocytosis. Clinical manifestation usually occurs up to the age of 2 years, with yellowish papules and variable clinical progression.
Pedro Henrique Oliveira Ribeiro, Laura Nagy Fritsch, Geraldo José Medeiros Fernandes, Adriano Macedo de Oliveira, Flávia Beatriz de Andrade Oliveira Ribeiro   +4 more
doaj   +1 more source

A case report of pediatric systemic juvenile xanthogranuloma

Malignancy Spectrum, Volume 2, Issue 1, Page 53-58, March 2025.
Abstract Background Juvenile xanthogranuloma (JXG) is a rare disorder that belongs to the broad group of non‐Langerhans cell histiocytosis. It is characterized by one or more nodules with predilection sites on the head, neck, and trunk, and lesions that may be several millimeters in diameter.
Feifei Liu, Man Hu, Rui Zhang, Zhigang Li, Hongyun Lian   +4 more
wiley   +1 more source

Xanthogranuloma of the sellar region

Medicine, 2020
Rationale: Xanthogranuloma of the sellar region is exceedingly rare, and described in only a handful of case reports. Herein, we present a case of xanthogranuloma of the sellar region to improve our knowledge for the diagnosis and management of this ...
X. Shao, Chao Wang, Jie Min
semanticscholar   +1 more source