Ritka betegségek ritka társulása: Langerhans-sejtes histiocytosis és lymphangioleiomyomatosis együttes elöfordulása a tüdöben.

Translated title of the contribution: Rare association of rare diseases: Langerhans-cell histiocytosis and lymphangioleiomyomatosis in the lung

Z. Márk, Z. Sápi, Z. Mészáros, J. Strausz

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

This is a case history of a 24-year-old female patient in whom two rare pulmonary diseases occurred: Langerhans cell histiocytosis and four years later lymphangioleiomyomatosis were diagnosed. Both diseases were verified by the examination of the lung tissue removed by the surgery for pneumothorax. The patient's symptoms were characterised by coughing, dyspnoe, repeated pneumothorax. The authors summarised the characteristics and treatment of these diseases. This case history is worth of reporting for its unique rareness.

Original languageHungarian
Pages (from-to)1851-1854
Number of pages4
JournalOrvosi Hetilap
Volume142
Issue number34
Publication statusPublished - Aug 26 2001

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Lymphangioleiomyomatosis
Langerhans Cell Histiocytosis
Pneumothorax
Rare Diseases
Lung
Lung Diseases
Therapeutics

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Ritka betegségek ritka társulása : Langerhans-sejtes histiocytosis és lymphangioleiomyomatosis együttes elöfordulása a tüdöben. / Márk, Z.; Sápi, Z.; Mészáros, Z.; Strausz, J.

In: Orvosi Hetilap, Vol. 142, No. 34, 26.08.2001, p. 1851-1854.

Research output: Contribution to journalArticle

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