Results 91 to 100 of about 24,931 (232)
Langerhans cell histiocytosis with hemorrhagic uveitis and exudative retinal detachment
, 2018 Ranju Kharel Sitaula,1 Anadi Khatri2 1Uveitis Department, B.P. Koirala Lions Center for Ophthalmic Studies, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal; 2Fellow of Vitreo-Retina Surgery, Lumbini Eye Institute, Siddharthanagar, Nepal ...
Kharel Sitaula R, Khatri A
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Pediatric Blood &Cancer, Volume 73, Issue 10, October 2026.ABSTRACT Juvenile xanthogranuloma (JXG) of the central nervous system (CNS) is a rare non‐Langerhans cell histiocytosis. CSF1R mutations have been reported for peripheral JXG, but not in CNS JXG. A 3‐month‐old male presented with fever, lymphadenopathy, and macrocephaly with bulging fontanelles.
Sima Vazquez +8 more
wiley +1 more source
Cutaneous Langerhans Cell Histiocytosis
, 2008 We report a 4-year-old boy with localized Langerhans cell histiocytosis. The lesions were restricted to the skin of his back, eyelids, glans penis and prepuce for 2 years. Histopathological and electron microscopic examinations showed typical features of
吳亮遠;蔡呈芳;陳佑甫;洪志明 +1 more
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The Clinical Respiratory JournalPulmonary Langerhans cell histiocytosis is a rare lung disease, which was previously classified as interstitial lung disease but is now classified as a myeloid neoplasm.
Jingyuan Fan +3 more
doaj +1 more source
A large multilobulated cutaneous nodule in infancy
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Hannah Wahida +2 more
wiley +1 more source
Langerhans Cell Histiocytosis (LCH) and Diabetes Insipidus with Mandibular lesion
, 2012 Langerhans cell histicytosis (LCH) is a rare disorder that primarily affects children. Its occurrence in adult is very rare. We report a case of 42 year old female patient who presented polyuria and polydipsia, loosing teeth and diplopia added to symptom
Sayeh Alizad jahani +3 more
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Clinical Case Reports, Volume 14, Issue 10, October 2026.ABSTRACT Gallbladder carcinoma is an aggressive malignancy often diagnosed at an advanced stage. Skeletal metastasis, especially mixed lytic‐sclerotic lesions, is rare and typically occurs late. This report highlights an unusual presentation where widespread bony metastases were the initial manifestation, leading to the diagnosis of gallbladder ...
Shivali Rao +2 more
wiley +1 more source
F105 Histiocytosis Infiltrate of Disc
, 1968 Histiocytosis infiltrate of right disc with simultaneous infiltration of the hypothalamus with skin lesions on eye lids and chest. Same patient as F1_06. Anatomy: Optic disc. Pathology: Histiocytosis infiltrate.
William F. Hoyt, MD
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Frontiers in OncologyBackgroundThe differential diagnosis of an adrenal mass is critical for clinical management. We report a case that expanded the spectrum of a rare disease and present a novel diagnostic trap for both pathologists and clinicians.MethodsHistopathological ...
Wenjing Ma +4 more
doaj +1 more source
Acta Medica, 2018 Langerhans cell histiocytosis (LCH) is a very rare disease in adults and as well a very rare cause of sellar expansion. The clinical presentation can be heterogeneous, from a single bone lesion to potentially fatal, widespread disease.
Filip Gabalec +9 more
doaj +1 more source