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Histiocytosis X: a clinical presentation
Author(s) -
McDonald J. S.,
Miller R. L.,
Bernstein M. L.,
Olson J. W.
Publication year - 1980
Publication title -
journal of oral pathology and medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.887
H-Index - 83
eISSN - 1600-0714
pISSN - 0904-2512
DOI - 10.1111/j.1600-0714.1980.tb00390.x
Subject(s) - diabetes insipidus , medicine , histiocytosis , histiocytosis x , differential diagnosis , langerhans cell histiocytosis , biopsy , presentation (obstetrics) , dermatology , pathology , radiology , disease , pediatrics
Abstract A 56‐year‐old male complained of chronic oral ulcers. Initial workup revealed diffuse alveolar bone destruction and other systemic disturbances including diabetes insipidus. Biopsy suggested histiocytosis X and further tests verified the diagnosis. A clinical differential diagnosis is developed, follow‐up is presented and the entities comprising histiocytosis X are discussed.

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