Langerhans cell histiocytosis, diabetes insipidus, hyperprolactinemia and empty sella: A four-fold association. Report of two cases

Author:

Panza N.,Merola B.,Colao A.,Lodice G.,de Bellis A.,Bizzarro A.,Bellastella A.,Lombardi Gaetano

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference21 articles.

1. Lichtenstein L. Histiocytosis X: integration of eosinophilic granuloma of bone, “Letterer Siwe disease”, and “Schuller - Christian disease” as related manifestations of a single nosologic entity. Arch Pathol. 56: 84, 1953.

2. The Writing Group of the Histiocyte Society. Histiocytosis syndromes in children. Lancet 1: 208, 1987.

3. Braustein G.D., Kohler P.O. Endocrine manifestations of histiocytosis. Am. J. Pediatr. Hematol. Oncol. 3: 67, 1991.

4. Matisonn R., Pimstone B. Diabetes insipidus associated with an empty sella turcica. Postgrad. Med. J. 48: 274, 1973.

5. Schaison G., Hetzger J. The primary empty sella: endocrine study of 12 cases. Acta Endocrinol. (Copenh.) 83: 483, 1976.

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