Abstract

Introduction: Myelodysplastic syndromes (MDS) are a group of haemopoietic stem cell disorders characterised by cytopenias and dysplasia in one or more myeloid cell lines with a risk of developing acute leukaemia. MDS can occur as a primary event or following exposure to chemotherapy or radiotherapy. Spontaneous remission can occur but is rare. Case Report : In this case report, a 39­year­old female developed MDS with a cytogenetic abnormality t (1;7) during treatment with cyclophosphamide for Wegener’s granulomatosis. A spontaneous morphological and cytogenetic remission occurred six years after initial diagnosis. Conclusion: Case reports of spontaneous remission in patients with primary MDS occasionally appear in the literature however there are very few reports concerning remission of therapy related MDS. This case is unusual as the patient achieved complete haematological and cytogenetic remission of treatment related MDS on a reduction of cyclophosphamide.

Highlights

  • Myelodysplastic syndromes (MDS) are a group of haemopoietic stem cell disorders characterised by cytopenias and dysplasia in one or more myeloid cell lines with a risk of developing acute leukaemia

  • MDS can occur as a primary event or following exposure to chemotherapy or radiotherapy

  • Mantadakis et al reported a series of five paediatric cases with MDS associated with monosomy 7 who had spontaneous haematological remission

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Summary

INTRODUCTION

Myelodysplastic syndromes (MDS) are a group of haemopoietic stem cell disorders characterised by cytopenias and dysplasia in one or more myeloid cell lines with a risk of developing acute leukaemia. Www.ijcasereportsandimages.com abnormalities improved, she developed psychiatric symptoms whilst taking steroids She was referred to a neurologist in a London based hospital in August 2000 who diagnosed her with Wegner’s Granulomatosis based on the clinical and laboratory findings with positive cytoplasmic antineutrophil cytoplasmic antibodies. She was commenced on cyclophosphamide 100 mg once a day and her visual evoked potentials normalised by 2003. By January 2007, the patient was transfusion independent and her complete blood count (CBC) was normalising Repeat bone marrow aspirate in September 2009 showed normal tri­lineage haemopoiesis and complete disappearance of t (1;7)

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