Skull Base Langerhans Cell Histiocytosis with Diabetes Insipidus and Panhypopituitarism- A Rare Clinical Entity

Skull Base Langerhans Cell Histiocytosis with Diabetes Insipidus and Panhypopituitarism- A Rare Clinical Entity

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Introduction A case of Langerhans cell histiocytosis (LGH) involving extensive area of base of skull resulting in panhypopituitarism and diabetes insipidus (DI) is reported. Case Report A 16 year old male presented with diminished vision, bilateral ptosis, left sided lateral rectus palsy,...

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Bibliographic Details
Main Authors: Anirban Ghosh, Mithun Chaudhury, Abhishek Mukherjee
Format: Article
Language:English
Published: The Association of Otolaryngologists of India, West Bengal 2017-12-01
Series:Bengal Journal of Otolaryngology and Head Neck Surgery
Subjects:
Myeloproliferative Disorders
Langerhans Cell Histiocytosis
Hypogonadism
Diabetes Insipidus
Skull Base
Online Access:https://bjohns.in/journal3/index.php/bjohns/article/view/145

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