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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.

Megaloblastic anemia

Anemia characterized by the presence of erythroblasts that are larger than normal (megaloblasts).

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PMID (PMCID)
20038929	MALE	Middle Aged
	Lymphocytic hypophysitis with dacryoadenitis in a male patient: non-invasive diagnosis and high-dose methylprednisolone pulse therapy.
	Lu Z, Li J, Ba J, Yang G, Dou J, Mu Y, Lu J. Neuro Endocrinol Lett. 2009;30(6):700-4.
	It is often detected in patients with other autoimmune systemic diseases such as Hashimoto's thyroiditis, epinephritis, megaloblastic anemia, and Langerhans cell histiocytosis.