Acute leukemia in association with Langerhans cell histiocytosis [PDF]
, 1994 Langerhans cell histiocytosis (LCH) and malignancy occurring in the same individual is unusual and has generally been the subject of isolated case reports.
Aricò, M. (Maurizio) +5 more
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Alternative genetic mechanisms of BRAF activation in Langerhans cell histiocytosis.
Blood, 2016 Langerhans cell histiocytosis (LCH) is characterized by inflammatory lesions containing pathologic CD207+ dendritic cells with constitutively activated ERK.
Rikhia Chakraborty +15 more
semanticscholar +1 more source
Langerhans cell sarcoma arising from antecedent langerhans cell histiocytosis
Medicine, 2019 Rationale: Langerhans cell sarcoma (LCS) is a rare, high-grade neoplasm characterized by overtly malignant cytologic features and a poor prognosis.
W. Yi +4 more
semanticscholar +1 more source
A rare cause of recurrent spontaneous pneumothorax: Birt-hogg-dube syndrome [PDF]
, 2018 Birt-Hogg-Dube (BHD) syndrome is an unusual disorder characterized by the triad of cutaneous lesions, renal tumors and lung cysts. In cases with BHD syndrome, the frequency of recurrent pneumothorax is increased due to presence of multiple lung cysts. It
Demirci, M. +3 more
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Langerhans cell histiocytosis with oral manifestations: a rare and unusual case report [PDF]
, 2012 Langerhans cell histiocytosis (LCH), is a rare, proliferative disorder in which the accumulation of pathologic Langerhans cells leads to local tissue infiltration and destruction.
Agarwal, Manjushree +2 more
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Langerhans cell histiocytosis (histiocytosis X) [PDF]
Postgraduate Medical Journal, 1997 Summary There has been a renewed interest in Langerhans cell histiocytosis in recent years due both to advances in basic research and to improvements in diagnostic and treatment approaches. In this article, we review the various aspects of the disease and the potential implications of these recent scientific researches for our ...
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Indeterminate Cell Histiocytosis: A Case Report [PDF]
, 2004 Indeterminate cell histiocytosis is a rare neoplasm composed of cells with mixed characteristics of Langerhans cells and non-Langerhans cells. An otherwise healthy, 36-year-old woman presented with asymptomatic generalized papules and nodules that had ...
Chen, Gwo-Shing, Wang, Chun-Hua
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Langerhans cell histiocytosis of the mandible: two case reports and literature review
Journal of the Korean Association of Oral and Maxillofacial Surgeons, 2019 Langerhans cell histiocytosis (LCH) is a rare disorder characterized by the proliferation of dendritic cells resulting in local or systemic symptoms. The clinical symptoms of patients with Langerhans cell histiocytosis depend on the site and the degree ...
Dae-Seok Hwang +7 more
semanticscholar +1 more source
Langerhans Cell Histiocytosis in a Newborn
Journal of the Chinese Medical Association, 2009 A full-term female baby was admitted to our hospital at the postnatal age of 37 days with generalized vesiculopapular, crateriform skin lesions. Physical examination revealed a well-nourished baby without fever, hepatosplenomegaly or lymphadenopathy. Laboratory examination was normal except for thrombocytosis (platelet count, 970 x 10(3)/microL).
Tzu Ying Yang +5 more
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Expression of Fas ligand in Langerhans' cell histiocytosis: A case report of a boy with multisystem involvement [PDF]
, 1999 Ching‐Tien Peng +6 more
openalex +2 more sources