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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.

Exertional dyspnea

Total: 1

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PMID (PMCID)
23417214	MIXED_SAMPLE	Adult
	[Pulmonary hypertension and Langerhans' cell granulomatosis: successful treatment with sildenafil and iloprost].
	Held M, Jany B, Warth A, Wilkens H. Dtsch Med Wochenschr. 2013;138(11):524-7.
	A 51-year-old woman (Case A) who had suffered from pulmonary Langerhans' cell granulomatosis for four years presented with progressive exertional dyspnea.