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Microangiopathic hemolytic anemia as an initial presentation of metastatic cancer of unknown primary origin

  • Yung Chang Lin
  • , Hsien Khun Chang
  • , Chien Feng Sun
  • , Lee Yung Shih*
  • *Corresponding author for this work
  • Chang Gung Memorial Hospital

Research output: Contribution to journalJournal Article peer-review

25 Scopus citations

Abstract

Microangiopathic hemolytic anemia (MAHA) is a well-documented but rare complication of disseminated cancer; it usually occurs in the late or terminal stage of cancer. We describe a case of metastatic carcinoma of unknown origin in which MAHA was the initial presentation. A 36-year-old woman came to our hospital with lower back pain and progressive exertional dyspnea for 8 weeks. Hemolytic anemia, thrombocytopenia, and leukoerythroblastosis were found on admission. The peripheral blood smear revealed polychromasia, poikilocytosis, and many schistocytes. Bone marrow biopsy disclosed metastatic carcinoma. After careful workup, we failed to find the primary site of cancer. The anemia and thrombocytopenia responded dramatically to combination chemotherapy with 5-fluorouracil, mitomycin C, and cisplatin. This case indicates that metastatic carcinoma should be included in the differential diagnosis in previously healthy patients with MAHA.

Original languageEnglish
Pages (from-to)683-687
Number of pages5
JournalSouthern Medical Journal
Volume88
Issue number6
DOIs
StatePublished - 06 1995
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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