BEYOND OF MORPHOLOGY DIAGNOSIS: A CASE REPORT OF PIODERMA GANGRENOSO AS THE FIRST MANIFESTATION OF MYELODYSPLASTIC NEOPLASIA

Introduction: Pyoderma gangrenosum can be the first cutaneous manifestation of paraneoplastic syndromes. Among the associated diseases include hematological malignancies. These disorders may have atypical clinical characteristics, with the association of Myelodysplastic Neoplasm (MDS) with the bullo...

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Main Authors: NFAM Mendonça, JVC Goes, FJAB Ribeiro, MA Viana, AA Vieira, RDB Dias, RFP Filho, NG Oliveira, RTG Oliveira, DP Borges, HLR Junior, SMM Magalhães, RF Pinheiro
Format: Article
Language:English
Published: Elsevier 2023-10-01
Series:Hematology, Transfusion and Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S2531137923010027
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author NFAM Mendonça
JVC Goes
FJAB Ribeiro
MA Viana
AA Vieira
RDB Dias
RFP Filho
NG Oliveira
RTG Oliveira
DP Borges
HLR Junior
SMM Magalhães
RF Pinheiro
author_facet NFAM Mendonça
JVC Goes
FJAB Ribeiro
MA Viana
AA Vieira
RDB Dias
RFP Filho
NG Oliveira
RTG Oliveira
DP Borges
HLR Junior
SMM Magalhães
RF Pinheiro
author_sort NFAM Mendonça
collection DOAJ
description Introduction: Pyoderma gangrenosum can be the first cutaneous manifestation of paraneoplastic syndromes. Among the associated diseases include hematological malignancies. These disorders may have atypical clinical characteristics, with the association of Myelodysplastic Neoplasm (MDS) with the bullous form being the most described and its appearance associated with poor prognosis. Objective: To report a case of skin lesion as a first manifestation of MDS. Case report: A 68-year-old woman started with fatigue and pain in the legs, evolving with the appearance of plaques with haemorrhagic blisters in the left calf and the presence of cytopenia was identified in laboratory tests (Haemoglobin 6.7 g/dL, leukocytes 2.300/mm3, and neutrophils 552/mm3, and platelets 95.000/mm3). Patient sought medical assistance and started a clinical investigation. During follow-up serologies were performed with all negative results. Myelogram was performed and immunophenotyping showed the presence of 18.7% of myeloid lineage blasts with aberrant CD7 marking. The patient was diagnosed with MDS, the treatment with dapsone was started, but the patient died a few months after diagnosis. Discussion: The diagnosis of pyoderma gangrenous is one of exclusion and other causes of ulcer disease should be investigated. Myelodysplastic Neoplasm should always be considered in patients with pyoderma gangrenosum accompanied by some mono, bi or pancytopenia and may appear at the same time with the hematological disease or, in its evolution, as a marker of malignant transformation. Conclusion: Myelodysplastic neoplasm should always be considered in patients with pyoderma gangrenosum accompanied by some cytopenia.
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spelling doaj.art-361eea7e2656490fadd1de4d02d75d852023-10-20T06:43:45ZengElsevierHematology, Transfusion and Cell Therapy2531-13792023-10-0145S442BEYOND OF MORPHOLOGY DIAGNOSIS: A CASE REPORT OF PIODERMA GANGRENOSO AS THE FIRST MANIFESTATION OF MYELODYSPLASTIC NEOPLASIANFAM Mendonça0JVC Goes1FJAB Ribeiro2MA Viana3AA Vieira4RDB Dias5RFP Filho6NG Oliveira7RTG Oliveira8DP Borges9HLR Junior10SMM Magalhães11RF Pinheiro12Cancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, BrazilPost-Graduate Program in Patology, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Patology, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Clinical Medicine Department, Universidade Federal do Ceará (UFC), Fortaleza, BrazilCancer Cytogenomic Laboratory, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Núcleo de Pesquisa e Desenvolvimento de Medicamentos (NPDM), Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Post-Graduate Program in Medical Science, Universidade Federal do Ceará (UFC), Fortaleza, Brazil; Clinical Medicine Department, Universidade Federal do Ceará (UFC), Fortaleza, BrazilIntroduction: Pyoderma gangrenosum can be the first cutaneous manifestation of paraneoplastic syndromes. Among the associated diseases include hematological malignancies. These disorders may have atypical clinical characteristics, with the association of Myelodysplastic Neoplasm (MDS) with the bullous form being the most described and its appearance associated with poor prognosis. Objective: To report a case of skin lesion as a first manifestation of MDS. Case report: A 68-year-old woman started with fatigue and pain in the legs, evolving with the appearance of plaques with haemorrhagic blisters in the left calf and the presence of cytopenia was identified in laboratory tests (Haemoglobin 6.7 g/dL, leukocytes 2.300/mm3, and neutrophils 552/mm3, and platelets 95.000/mm3). Patient sought medical assistance and started a clinical investigation. During follow-up serologies were performed with all negative results. Myelogram was performed and immunophenotyping showed the presence of 18.7% of myeloid lineage blasts with aberrant CD7 marking. The patient was diagnosed with MDS, the treatment with dapsone was started, but the patient died a few months after diagnosis. Discussion: The diagnosis of pyoderma gangrenous is one of exclusion and other causes of ulcer disease should be investigated. Myelodysplastic Neoplasm should always be considered in patients with pyoderma gangrenosum accompanied by some mono, bi or pancytopenia and may appear at the same time with the hematological disease or, in its evolution, as a marker of malignant transformation. Conclusion: Myelodysplastic neoplasm should always be considered in patients with pyoderma gangrenosum accompanied by some cytopenia.http://www.sciencedirect.com/science/article/pii/S2531137923010027
spellingShingle NFAM Mendonça
JVC Goes
FJAB Ribeiro
MA Viana
AA Vieira
RDB Dias
RFP Filho
NG Oliveira
RTG Oliveira
DP Borges
HLR Junior
SMM Magalhães
RF Pinheiro
BEYOND OF MORPHOLOGY DIAGNOSIS: A CASE REPORT OF PIODERMA GANGRENOSO AS THE FIRST MANIFESTATION OF MYELODYSPLASTIC NEOPLASIA
Hematology, Transfusion and Cell Therapy
title BEYOND OF MORPHOLOGY DIAGNOSIS: A CASE REPORT OF PIODERMA GANGRENOSO AS THE FIRST MANIFESTATION OF MYELODYSPLASTIC NEOPLASIA
title_full BEYOND OF MORPHOLOGY DIAGNOSIS: A CASE REPORT OF PIODERMA GANGRENOSO AS THE FIRST MANIFESTATION OF MYELODYSPLASTIC NEOPLASIA
title_fullStr BEYOND OF MORPHOLOGY DIAGNOSIS: A CASE REPORT OF PIODERMA GANGRENOSO AS THE FIRST MANIFESTATION OF MYELODYSPLASTIC NEOPLASIA
title_full_unstemmed BEYOND OF MORPHOLOGY DIAGNOSIS: A CASE REPORT OF PIODERMA GANGRENOSO AS THE FIRST MANIFESTATION OF MYELODYSPLASTIC NEOPLASIA
title_short BEYOND OF MORPHOLOGY DIAGNOSIS: A CASE REPORT OF PIODERMA GANGRENOSO AS THE FIRST MANIFESTATION OF MYELODYSPLASTIC NEOPLASIA
title_sort beyond of morphology diagnosis a case report of pioderma gangrenoso as the first manifestation of myelodysplastic neoplasia
url http://www.sciencedirect.com/science/article/pii/S2531137923010027
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