Treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome case

Umit Yavuz Malkan, Gursel Gunes, Eylem Eliacik, Ibrahim Celalettin Haznedaroglu Department of Hematology, School of Medicine, Hacettepe University, Ankara, Turkey Abstract: Thalidomide may be used as a treatment option for pyoderma gangrenosum (PG) and myelodysplastic syndrome (MDS). Herein, we aim...

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Main Authors: Malkan UY, Gunes G, Eliacik E, Haznedaroglu IC
Format: Article
Language:English
Published: Dove Medical Press 2016-03-01
Series:International Medical Case Reports Journal
Subjects:
Online Access:https://www.dovepress.com/treatment-of-pyoderma-gangrenosum-with-thalidomide-in-a-myelodysplasti-peer-reviewed-article-IMCRJ
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spelling doaj-5e95474825d446d2b3077b21d0e048c52020-11-25T01:08:49ZengDove Medical PressInternational Medical Case Reports Journal1179-142X2016-03-012016Issue 1616426039Treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome caseMalkan UYGunes GEliacik EHaznedaroglu ICUmit Yavuz Malkan, Gursel Gunes, Eylem Eliacik, Ibrahim Celalettin Haznedaroglu Department of Hematology, School of Medicine, Hacettepe University, Ankara, Turkey Abstract: Thalidomide may be used as a treatment option for pyoderma gangrenosum (PG) and myelodysplastic syndrome (MDS). Herein, we aimed to report a patient who was treated well with thalidomide and whose diagnosis was PG with MDS. A 61-year-old man with painless ecchymotic lesions in his right upper extremity was admitted to the hospital in Isparta, Turkey, in January 2015. The lesions were diagnosed as PG. In his anamnesis, it was found that he was diagnosed with MDS 6 years ago and had been treated with cyclosporine at 2×100 mg for 5 years, which was stopped in January 2015. Aspiration from liver lesion revealed the presence of Mycobacterium tuberculosis, so antituberculosis treatment was started. Bone marrow investigation revealed MDS-refractory anemia with excess blasts (7%). For lesions in bilateral upper extremities, thalidomide treatment was started at 50 mg/d. After 1 month from the initiation of thalidomide treatment, the lesions in upper extremities had disappeared. In the literature, there are some reports of patients with PG who were successfully treated with thalidomide. Our patient is a complicated case who simultaneously has MDS, PG, and tuberculosis infection. The reason for thalidomide usage in our patient was the need of immune modulation without immune suppression. Our patient has tolerated the drug well, and excellent response was obtained after 1 month of initiation of thalidomide treatment. To conclude, thalidomide is a very effective drug acting as an immune modulator, which is useful in the clinical management of both MDS and PG. Keywords: pyoderma gangrenosum, thalidomide, myelodysplastic syndromehttps://www.dovepress.com/treatment-of-pyoderma-gangrenosum-with-thalidomide-in-a-myelodysplasti-peer-reviewed-article-IMCRJPyoderma GangrenosumThalidomideMyelodysplastic syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Malkan UY
Gunes G
Eliacik E
Haznedaroglu IC
spellingShingle Malkan UY
Gunes G
Eliacik E
Haznedaroglu IC
Treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome case
International Medical Case Reports Journal
Pyoderma Gangrenosum
Thalidomide
Myelodysplastic syndrome
author_facet Malkan UY
Gunes G
Eliacik E
Haznedaroglu IC
author_sort Malkan UY
title Treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome case
title_short Treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome case
title_full Treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome case
title_fullStr Treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome case
title_full_unstemmed Treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome case
title_sort treatment of pyoderma gangrenosum with thalidomide in a myelodysplastic syndrome case
publisher Dove Medical Press
series International Medical Case Reports Journal
issn 1179-142X
publishDate 2016-03-01
description Umit Yavuz Malkan, Gursel Gunes, Eylem Eliacik, Ibrahim Celalettin Haznedaroglu Department of Hematology, School of Medicine, Hacettepe University, Ankara, Turkey Abstract: Thalidomide may be used as a treatment option for pyoderma gangrenosum (PG) and myelodysplastic syndrome (MDS). Herein, we aimed to report a patient who was treated well with thalidomide and whose diagnosis was PG with MDS. A 61-year-old man with painless ecchymotic lesions in his right upper extremity was admitted to the hospital in Isparta, Turkey, in January 2015. The lesions were diagnosed as PG. In his anamnesis, it was found that he was diagnosed with MDS 6 years ago and had been treated with cyclosporine at 2×100 mg for 5 years, which was stopped in January 2015. Aspiration from liver lesion revealed the presence of Mycobacterium tuberculosis, so antituberculosis treatment was started. Bone marrow investigation revealed MDS-refractory anemia with excess blasts (7%). For lesions in bilateral upper extremities, thalidomide treatment was started at 50 mg/d. After 1 month from the initiation of thalidomide treatment, the lesions in upper extremities had disappeared. In the literature, there are some reports of patients with PG who were successfully treated with thalidomide. Our patient is a complicated case who simultaneously has MDS, PG, and tuberculosis infection. The reason for thalidomide usage in our patient was the need of immune modulation without immune suppression. Our patient has tolerated the drug well, and excellent response was obtained after 1 month of initiation of thalidomide treatment. To conclude, thalidomide is a very effective drug acting as an immune modulator, which is useful in the clinical management of both MDS and PG. Keywords: pyoderma gangrenosum, thalidomide, myelodysplastic syndrome
topic Pyoderma Gangrenosum
Thalidomide
Myelodysplastic syndrome
url https://www.dovepress.com/treatment-of-pyoderma-gangrenosum-with-thalidomide-in-a-myelodysplasti-peer-reviewed-article-IMCRJ
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