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Spontaneous pneumothorax with isolated pulmonary Langerhans cell histiocytosis in an adult case: A common manifestation of rare disease.
Samareh Fekri, Mitra; Salajegheh, Faranak; Nakhaie, Mohsen; Rezaei Zadeh Rukerd, Mohammad.
Afiliação
  • Samareh Fekri M; Cardiovascular Research Center Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences Kerman Iran.
  • Salajegheh F; Clinical Research Development Unit, School of Medicine Afzalipour Hospital, Kerman University of Medical Sciences Kerman Iran.
  • Nakhaie M; Gastroenterology and Hepatology Research Center Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences Kerman Iran.
  • Rezaei Zadeh Rukerd M; Gastroenterology and Hepatology Research Center Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences Kerman Iran.
Clin Case Rep ; 11(6): e7567, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37334339
ABSTRACT
Key Clinical Message Pulmonary Langerhans cell histiocytosis should be evaluated even in adults with no previous medical history and no history of cigarette smoking who have spontaneous pneumothorax and evidence of multiple lung cystic lesions, and other organs should also be checked for multi organ Langerhans cell histiocytosis involvement. Abstract A 30-year-old man presented with sudden chest pain and evidence of multiple cystic lesions in both upper and lower lobes of lungs, as well as left-sided pneumothorax in high resolution computed tomography. In lung samples, hematoxylin and eosin- stained sections and IHC for CD1a, S100, and BRAF V600 were positive. The patient was diagnosed with isolated pulmonary Langerhans cell histiocytosis and was treated accordingly.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2023 Tipo de documento: Article