Miliary Tuberculosis in a Young Woman with Hemophagocytic Syndrome: A Case Report and Literature Review

نویسندگان

  • Mina Asaji
  • Kazunori Tobino
  • Koujin Murakami
  • Yuki Goto
  • Takuto Sueyasu
  • Saori Nishizawa
  • Kohei Yoshimine
  • Miyuki Munechika
  • Yuki Ko
  • Yuki Yoshimatsu
  • Kosuke Tsuruno
  • Hiromi Ide
  • Hiroyuki Miyajima
  • Noriyuki Ebi
چکیده

We herein report a rare case of miliary tuberculosis-associated hemophagocytic syndrome (HPS) complicated with respiratory failure. A 19-year-old Japanese woman with a fever, general malaise, and chest radiograph abnormalities was referred to our hospital. After admission, she developed respiratory failure with pancytopenia. A histological examination of lung and bone marrow biopsy samples revealed noncaseating granulomas without evidence of acid-fast bacilli or lymphoma. In addition, a bone marrow biopsy showed marked histiocyte hyperplasia with hemophagocytosis, and a bronchoalveolar lavage fluid culture grew Mycobacterium tuberculosis. Therefore, a diagnosis of miliary tuberculosis-associated HPS was made. The patient was successfully treated with antituberculous therapy.

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عنوان ژورنال:

دوره 56  شماره 

صفحات  -

تاریخ انتشار 2017