Results 91 to 100 of about 5,574,084 (164)
A report of radiographic manifestations of 32 patients with Histiocytosis X
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2001 Objective: Histiocytosis-X (H-X) is more common in children who are under 12 years. It involves different organs such as bone, lung, liver, spleen and skin.
N Ghojeh Vand, M Nabahati
doaj
Hepatic sinusoidal dilation in the course of histiocytosis X
, 1983 We present a case of disseminated histiocytosis X with hepatic involvement characterized by sinusoidal dilation. This histological feature regressed in connection with the clinical remission of the disease.
VAJRO, Pietro +4 more
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Langerhans cell histiocytosis in monocygote twins: case reports.
, 1996 Langerhans cell histiocytosis includes three clinical forms of histiocytosis X. We describe a disseminated form of Langerhans cell histiocytosis (Letterer-Siwe disease) in monozygotic twins.
Mader I +3 more
core +1 more source
Langerhans cell histiocytosis of the sphenoid sinus: a case report
The Turkish Journal of Pediatrics, 2010 Langerhans cell histiocytosis (LCH), previously known as histiocytosis X, is a rare disorder characterized by clonal proliferation and excess accumulation of pathologic Langerhans cells causing local or systemic effects.
Guohua Yu +5 more
doaj
Plenary Abstracts Session & Oral Presentations
HemaSphere, Volume 10, Issue S1, June 2026.
wiley +1 more source
, 1990 The gastrointestinal tract may be involved in Langerhans' cell histiocytosis, either as part of a generalized disease or as a separate primary entity. Three patients with gastrointestinal involvement are described. One patient presented with a history of
Schipper, M. E. +2 more
core +1 more source
Langerhans’ cell histiocytosis (histiocytosis X): A rare and diverse group of disorder in children [PDF]
, 2017 Langerhans cell histiocytosis is a rare disorder of unknown etiology with proliferation of Langerhans’ cells which may infiltrate a single or multiple organs.
Prajapati, Snehal +2 more
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