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Case Rep Oncol. 2015 Jun 05;8(2):256-63. doi: 10.1159/000431213. eCollection 2015.

Metastatic Breast Cancer with Extensive Osseous Metastasis Presenting with Symptomatic Immune Thrombocytopenic Purpura and Anemia: A Case Report and Review of the Literature.

Case reports in oncology

Jiaxin Niu, Teresa Goldin, Maurie Markman, Madappa N Kundranda

Affiliations

  1. Department of Medical Oncology, Western Regional Medical Center at Cancer Treatment Centers of America, Goodyear, Ariz., USA.
  2. Department of Pathology, Western Regional Medical Center at Cancer Treatment Centers of America, Goodyear, Ariz., USA.
  3. Department of Medical Oncology, Cancer Treatment Centers of America, Drexel University College of Medicine, Philadelphia, Pa., USA ; Drexel University College of Medicine, Philadelphia, Pa., USA.

PMID: 26120311 PMCID: PMC4478340 DOI: 10.1159/000431213

Abstract

BACKGROUND: Immune thrombocytopenic purpura (ITP) is a rare acquired bleeding disorder with an estimated incidence of 1 in 10,000 people in the general population. The association of ITP with breast cancer is an even rarer entity with very limited reports in the English literature.

CASE PRESENTATION: We report a case of a 51-year-old female with no significant past medical history who presented with sudden onset of malaise, syncope, gingival bleed and epistaxis. She was found to have severe thrombocytopenia (platelet count 6,000/μl) and anemia (hemoglobin 7.2 g/dl). Her workup led to the diagnosis of metastatic ductal breast cancer with extensive bone metastasis. Bone marrow biopsy demonstrated myelophthisis which was initially thought to be consistent with her presentation of thrombocytopenia and anemia. Therefore, the patient was started on hormonal therapy for the treatment of her metastatic breast cancer. After 3 months of therapy, she did not improve and developed severe mucosal bleeding. Her clinical presentation was suspicious for ITP and immune-mediated anemia, and hence she was started on steroids and intravenous immunoglobulin. The patient had a dramatic response to therapy with normalization of her platelet count and hemoglobin within 2 weeks.

CONCLUSION: To our knowledge, this is the first reported case of metastatic breast cancer presenting with symptomatic ITP and anemia, and both symptoms are postulated to be immune-mediated.

Keywords: Anemia; Bone metastasis; Breast cancer; Idiopathic thrombocytopenic purpura

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