Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Hypopituitarism



合計: 3

                       


（表示件数）
PMID (PMCID)
25873887
(4386111)
 OTHER
Langerhans cell histiocytosis in an adult with involvement of the calvarium, cerebral cortex and brainstem: discussion of pathophysiology and rationale for the use of intravenous immune globulin.
Dardis C, Aung T, Shapiro W, Fortune J, Coons S.
Case Rep Neurol. 2015;7(1):30-8.
We report a case of Langerhans cell histiocytosis in a 64-year-old male who presented with symptoms and signs of brain involvement, including seizures and hypopituitarism.
11686544
 MIXED_SAMPLE Child
Hypopituitarism in langerhans cell histiocytosis: seven cases and literature review.
Modan-Moses D, Weintraub M, Meyerovitch J, Segal-Lieberman G, Bielora B.
J Endocrinol Invest. 2001;24(8):612-7.
Hypopituitarism in langerhans cell histiocytosis: seven cases and literature review.
3873933
 FEMALE Adult
Primary hypothyroidism and essential hypernatremia in a patient with histiocytosis X.
Ma JT, Ho FC, Wang C, Lam KS, Yeung RT.
Aust N Z J Med. 1985;15(1):72-4.
Endocrine tests showed the presence of hypopituitarism and a discrete suprasellar mass, consistent with hypothalamic histiocytosis X, was demonstrated by computerised tomography.