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Acute Panmyelosis with Myelofibrosis - A Rare Subtype of Acute Myeloid Leukemia
One case of acute panmyelosis with myelofibrosis (APMF) is here reported. A 45 year old male presented with abrupt onset of rapidly progressing low backache, weakness and pancytopenia. On examination there was no organomegaly. Peripheral blood examination revealed normocytic normochromic red blood c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Università Cattolica del Sacro Cuore
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684347/ https://www.ncbi.nlm.nih.gov/pubmed/23795280 http://dx.doi.org/10.4084/MJHID.2013.042 |
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author | Chatterjee, Tathagata Gupta, Srishti Sharma, Ajay Sharma, Sanjeevan Gupta, Devika |
author_facet | Chatterjee, Tathagata Gupta, Srishti Sharma, Ajay Sharma, Sanjeevan Gupta, Devika |
author_sort | Chatterjee, Tathagata |
collection | PubMed |
description | One case of acute panmyelosis with myelofibrosis (APMF) is here reported. A 45 year old male presented with abrupt onset of rapidly progressing low backache, weakness and pancytopenia. On examination there was no organomegaly. Peripheral blood examination revealed normocytic normochromic red blood cells with 10% circulating blasts. Flowcytometric examination of peripheral blood revealed blasts which were positive for CD34, HLA− DR and myeloid associated antigens (i.e. CD13 and CD33). Blasts were negative for anti MPO. Bone marrow aspirate resulted in a dry tap. Bone marrow biopsy revealed panmyeloid proliferation with scattered blasts which were CD34 positive on imunohistochemistry and negative for anti MPO. Reticulin stain showed grade III myelofibrosis (WHO). Differential diagnosis considered included AML-M7, MDS-RAEB II and AML with myelodysplasia. He was started on chemotherapy [idarubicin and cytarabine; 3+7 induction regimen followed by three cycles of HIDAC (High dose cytosine arabinoside)] after which patient was in complete morphological remission with markedly reduced bone marrow fibrosis. He is now being worked up for allogeneic stem cell transplantation. Patient is asymptomatic at eight months of diagnosis. In conclusion these patients should be managed aggressively with AML therapy and this case report reaffirms the fact that APMF is subtype of AML. |
format | Online Article Text |
id | pubmed-3684347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Università Cattolica del Sacro Cuore |
record_format | MEDLINE/PubMed |
spelling | pubmed-36843472013-06-21 Acute Panmyelosis with Myelofibrosis - A Rare Subtype of Acute Myeloid Leukemia Chatterjee, Tathagata Gupta, Srishti Sharma, Ajay Sharma, Sanjeevan Gupta, Devika Mediterr J Hematol Infect Dis Case Report One case of acute panmyelosis with myelofibrosis (APMF) is here reported. A 45 year old male presented with abrupt onset of rapidly progressing low backache, weakness and pancytopenia. On examination there was no organomegaly. Peripheral blood examination revealed normocytic normochromic red blood cells with 10% circulating blasts. Flowcytometric examination of peripheral blood revealed blasts which were positive for CD34, HLA− DR and myeloid associated antigens (i.e. CD13 and CD33). Blasts were negative for anti MPO. Bone marrow aspirate resulted in a dry tap. Bone marrow biopsy revealed panmyeloid proliferation with scattered blasts which were CD34 positive on imunohistochemistry and negative for anti MPO. Reticulin stain showed grade III myelofibrosis (WHO). Differential diagnosis considered included AML-M7, MDS-RAEB II and AML with myelodysplasia. He was started on chemotherapy [idarubicin and cytarabine; 3+7 induction regimen followed by three cycles of HIDAC (High dose cytosine arabinoside)] after which patient was in complete morphological remission with markedly reduced bone marrow fibrosis. He is now being worked up for allogeneic stem cell transplantation. Patient is asymptomatic at eight months of diagnosis. In conclusion these patients should be managed aggressively with AML therapy and this case report reaffirms the fact that APMF is subtype of AML. Università Cattolica del Sacro Cuore 2013-06-04 /pmc/articles/PMC3684347/ /pubmed/23795280 http://dx.doi.org/10.4084/MJHID.2013.042 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Chatterjee, Tathagata Gupta, Srishti Sharma, Ajay Sharma, Sanjeevan Gupta, Devika Acute Panmyelosis with Myelofibrosis - A Rare Subtype of Acute Myeloid Leukemia |
title | Acute Panmyelosis with Myelofibrosis - A Rare Subtype of Acute Myeloid Leukemia |
title_full | Acute Panmyelosis with Myelofibrosis - A Rare Subtype of Acute Myeloid Leukemia |
title_fullStr | Acute Panmyelosis with Myelofibrosis - A Rare Subtype of Acute Myeloid Leukemia |
title_full_unstemmed | Acute Panmyelosis with Myelofibrosis - A Rare Subtype of Acute Myeloid Leukemia |
title_short | Acute Panmyelosis with Myelofibrosis - A Rare Subtype of Acute Myeloid Leukemia |
title_sort | acute panmyelosis with myelofibrosis - a rare subtype of acute myeloid leukemia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684347/ https://www.ncbi.nlm.nih.gov/pubmed/23795280 http://dx.doi.org/10.4084/MJHID.2013.042 |
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