Abstract
We present a 74-year-old woman with a recent diagnosis of myelodysplastic syndrome who presented with left upper quadrant abdominal pain and fatigue with significant splenomegaly, anemia, and thrombocytopenia. She underwent splenectomy and bone marrow biopsy. Pathology of both spleen and bone marrow revealed an unusual diagnosis. A review of the differential diagnosis, laboratory tests, nature of the underlying disease, and treatment are provided.
Original language | English (US) |
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Pages (from-to) | 252-257 |
Number of pages | 6 |
Journal | Allergy and Asthma Proceedings |
Volume | 31 |
Issue number | 3 |
DOIs | |
State | Published - May 2010 |
Keywords
- D816V
- Hematologic non-mast cell lineage disease
- Hypersplenism
- Mast cells
- Mastocytosis
- Myelodysplastic syndrome
- Splenomegaly
- Systemic mastocytosis with associated clonal
- Urticaria pigmentosa
ASJC Scopus subject areas
- Immunology and Allergy
- Pulmonary and Respiratory Medicine