Results 51 to 60 of about 7,890 (255)
J Pediatr Gastroenterol Nutr. 2005 Oct;41(4):483-4, 484. Clinical quiz. Prior AC, Selores M, Pina R, Dias JA, Costa FM, Vale L, Gomes L. Department of Pediatrics, Hospital Geral de Santo António, Portugal.
COSTA, F.M. +6 more
core +1 more source
A rare case of xanthogranuloma of the stomach masquerading as an advanced stage tumor
Background Xanthogranuloma of the stomach is an extremely rare disease, and this lesion has only been found to coexist with early gastric cancer in 2 cases in the literature.
Arii Kazuo +5 more
doaj +1 more source
The histiocytoses are a heterogenous group of diseases that are characterized by the accumulation of reactive or neoplastic histiocytes in various tissues.
L. Lama, B.M.M.K. Kayastha, R. Tripathi
doaj +3 more sources
Lingual juvenile xanthogranuloma in a woman: a case report
Introduction Juvenile xanthogranuloma is a rare non-Langerhans cell histiocytosis that usually occurs during infancy and early childhood. The presence of single or multiple raised cutaneous lesions characterize this self-healing disorder.
Villa Francesco +2 more
doaj +1 more source
Multiple generalized xanthogranuloma in adult: Case report and treatment
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 +3 more
doaj +1 more source
Inflammatory myofibroblastic tumor of the lung- a case report [PDF]
A 45-year-old man presented with a six-month history of progressive dyspnea with productive cough and wheezing. The patient was a heavy smoker and had a history of tongue cancer, hypertension, and asthma. Chest X-ray and computed tomography showed a mass
Chien-Kuang Chen +7 more
core +1 more source
ABSTRACT Multiple myeloma (MM) is a malignant plasma cell disorder that primarily presents with CRAB symptoms (calcium elevation, renal failure, anemia, and bone abnormalities). In rare cases, MM manifests with systemic complications like skin ulcers, which present management challenges. Here, we report a 78‐year‐old Japanese man with MM and refractory
Naoko Hattori +5 more
wiley +1 more source
Juvenile Xanthogranuloma: Case Report and Literature Review
Juvenile Xanthogranuloma (JXG) is a relatively uncommon non-Langerhans cell histiocytosis, which often occurs at an early age and is usually asymptomatic.
Sadegh Vahabi-Amlashi +2 more
semanticscholar +1 more source
Cutaneous necrobiotic xanthogranuloma (NXG)--successfully treated with low dose chlorambucil. [PDF]
Eur J Dermatol. 2001 Sep-Oct;11(5):458-62. Cutaneous necrobiotic xanthogranuloma (NXG)--successfully treated with low dose chlorambucil. Machado S, Alves R, Lima M, Leal I, Massa A.
Alves, R. +4 more
core
Juvenile xanthogranuloma (JXG) usually presents with lesions isolated to the skin; however, aggressive, disseminated forms also occur. Identification of a novel MRC1-PDGFRB fusion in a child with JXG guided targeted therapy with dasatinib, leading to a
S. Eissa +8 more
semanticscholar +1 more source

