A rare case of solitary brain Langerhans cell histiocytosis with intratumoral hemorrhage in a patient affected by Turner syndrome

Rosa Morabito; Giovanni Grasso; Francesca Granata; Rosa Morabito; Elisabetta Alafaci; Concetta Alafaci; Francesco M. Salpietro; Francesca Granata

A rare case of solitary brain Langerhans cell histiocytosis with intratumoral hemorrhage in a patient affected by Turner syndrome

Rosa Morabito, Giovanni Grasso, Francesca Granata, Rosa Morabito, Elisabetta Alafaci, Concetta Alafaci, Francesco M. Salpietro, Francesca Granata

Biomedicina, Neuroscienze e Diagnostica avanzata

Risultato della ricerca: Article › peer review

Abstract

Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of cells with characteristics similar to bone marrow-derived Langerhans cells. The case of a young woman, affected by Turner syndrome and a solitary intraparenchymal LCH associated with an osteolytic lesion of the overlying skull, is presented.

Lingua originale	English
pagine (da-a)	31-
Numero di pagine	6
Rivista	SURGICAL NEUROLOGY INTERNATIONAL
Volume	7
Stato di pubblicazione	Published - 2016

All Science Journal Classification (ASJC) codes

Surgery
Clinical Neurology

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A rare case of solitary brain Langerhans cell histiocytosis with intratumoral hemorrhage in a patient affected by Turner syndrome. / Morabito, Rosa ; Grasso, Giovanni; Granata, Francesca; Morabito, Rosa; Alafaci, Elisabetta; Alafaci, Concetta; Salpietro, Francesco M.; Granata, Francesca.

In: SURGICAL NEUROLOGY INTERNATIONAL, Vol. 7, 2016, pag. 31-.

Risultato della ricerca: Article › peer review

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AU - Alafaci, Elisabetta

AU - Alafaci, Concetta

AU - Salpietro, Francesco M.

AU - Granata, Francesca

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AB - Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of cells with characteristics similar to bone marrow-derived Langerhans cells. The case of a young woman, affected by Turner syndrome and a solitary intraparenchymal LCH associated with an osteolytic lesion of the overlying skull, is presented.

UR - http://hdl.handle.net/10447/191330

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