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Presse medicale (Paris, France : 1983) · 2006

[Hypothalamic-pituitary Langerhans cell histiocytosis in adults].

Клинический случайАннотация на английскомСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Essais Olfa, Jomaa Rached, Bougerra Radhia, Marrakchi Zinet, Ben Salem Leila, Ouertani Haroun, Chamakhi Saïd, Neji Sonia, Ben Slama Claude, Zidi Borni

Аннотация

INTRODUCTION: Langerhans cell histiocytosis is a rare entity. Involvement of the pituitary region is frequently delayed and rarely studied.

CASES: We report some clinical and paraclinical particularities of the disease in four women. Diabetes insipidus was the initial symptom in all cases, accompanied by panhypopituitarism at initial presentation in one woman. Hypopituitarism was diagnosed from 6 months to 4 years after the diabetes insipidus in the other cases, and systemic lesions appeared 3 to 6 years thereafter. Magnetic resonance imaging of the hypothalamic-pituitary axis found tumors in two patients and infundibular thickening in the other two. One patient also had a partially empty sella.

DISCUSSION: In adults, pituitary involvement seems to occur predominantly in women, and panhypopituitarism is possible at initial presentation. The clinical polymorphism of Langerhans cell histiocytosis makes this disease difficult and often slow to diagnose.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты