Results 91 to 100 of about 4,921,178 (191)

Langerhans cell histiocytosis presenting as eosinophilic granuloma of the bilateral forearms in an 8-year-old girl: a case report

open access: yesJournal of Medical Case Reports, 2019
Background Langerhans cell histiocytosis previously known as histiocytosis X is a rare disease of children and young adults with a very broad clinical spectrum. In children, its annual incidence is estimated between 0.2–0.5 per 100,000.
Salahoudine Idrissa   +6 more
doaj   +1 more source

Occult Langerhans Cell Histiocytosis in Clear Cell Renal Cell Carcinoma

open access: yes, 2017
Langerhans cell histiocytosis is a rare disease that is characterized by a localized or systemic proliferation of Langerhans dendritic cells and a wide spectrum of clinical presentations.
Phil Hyun Song, Mi Jin Gu, Hee Jung Kwon
core   +1 more source

Endocrine manifestations in Langerhans cell histiocytosis.

open access: yes, 2007
Langerhans cell histiocytosis is a rare, multisystem disease that shows a particular predilection for hypothalamo-pituitary axis involvement. Diabetes insipidus is the most frequent permanent consequence of Langerhans cell histiocytosis, developing in ...
Chrousos, GP   +4 more
core   +3 more sources

Perifollicular Langerhans cell histiocytosis

open access: yesDermatology Online Journal, 2012
A 25-year-old man presented with a 13-year history of an erythematous, papular eruption of his face and trunk, which was treated in the past as acne and psoriasis with isotretinoin and methotrexate, respectively. Histopathologic examination demonstrated an infiltrate of Langerhans cells, which was consistent with Langerhans cell histiocytosis.
Mir, Adnan   +3 more
openaire   +4 more sources

Cutaneous Langerhans Cell Histiocytosis

open access: yes, 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
core  

Histiocytosis X: Langerhans’ Cell Histiocytosis

open access: yesHematology/Oncology Clinics of North America, 1987
Histiocytosis X is a complex and poorly understood entity. Nevertheless, it would appear as if certain themes are found recurrently throughout the literature dealing with this disease and a review of them serves as a useful summary. 1. Problems with Nomenclature.
openaire   +2 more sources

Insights into etiology and management of a case of Langerhans cell histiocytosis manifesting as perianal lesions: a case report

open access: yesJournal of Medical Case Reports
Background Langerhans cell histiocytosis is a rare disorder characterized by abnormal proliferation of Langerhans cells, primarily affecting children and occasionally adults.
Pei Xiao-yue, Tai Zixin, Zhang Wen-jun
doaj   +1 more source

EXPRESSION OF ADHESION MOLECULES IN LANGERHANS CELL HISTIOCYTOSIS

open access: yes, 1993
Expression of adhesion molecules was investigated in six biopsy specimens of Langerhans' cell histiocytosis using immunocytochemistry. Cells with Langerhans' cell histiocytosis morphology were stained for ICAM-1, for the beta-1 integrins alpha-4 (VLA-4 ...
C.D. BARONI   +8 more
core   +1 more source

Langerhans cell histiocytosis: a diagnostic dilemma

open access: yes, 2012
Langerhans cell histiocytosis (LCH) is a rare clonal neoplastic disorder of unknown aetiology which can present with a diverse range of clinical presentations.
Paul L Ryan   +5 more
core   +1 more source

Systemic findings of Langerhans cell histiocytosis in neonatal period

open access: yesRevista de la Facultad de Ciencias de la Salud, 2011
We report an unusual case of mediastinal abcessed mass, with involvement of the lung, thymus and probably bone and hematopoietic system, in a newborn that was diagnosed with Langerhans cell histiocytosis.
Rosalba Días-Castro   +6 more
doaj   +2 more sources

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