Waldenstrom’s Macroglobulinemia and Peripheral Neuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes with a Bleeding Diathesis and Rash
We report a case of a 29-year-old male who presented with paraesthesia and skin lesions with excessive bleeding after skin biopsy leading to hematology consultation. He was found to have prolonged partial thromboplastin time (PTT) and monoclonal gammopathy on serum protein electrophoresis (SPEP). He...
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Online Access: | http://dx.doi.org/10.1155/2013/890864 |
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doaj-f4e2a4b0a4b24acc911239cff6d44b882020-11-24T23:18:07ZengHindawi LimitedCase Reports in Oncological Medicine2090-67062090-67142013-01-01201310.1155/2013/890864890864Waldenstrom’s Macroglobulinemia and Peripheral Neuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes with a Bleeding Diathesis and RashS. Haider0T. Latif1A. Hochhausler2F. Lucas3N. Abdel Karim4Department of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USADepartment of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USADepartment of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USADepartment of Pathology, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USADepartment of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USAWe report a case of a 29-year-old male who presented with paraesthesia and skin lesions with excessive bleeding after skin biopsy leading to hematology consultation. He was found to have prolonged partial thromboplastin time (PTT) and monoclonal gammopathy on serum protein electrophoresis (SPEP). He experienced excessive bleeding leading to hospitalization after bone marrow biopsy and required blood transfusion. He was diagnosed with Waldenstrom's Macroglobulinemia (WM), based on the presence of IgM-κ type monoclonal (M) protein and infiltration of lymphoplasmacytic cells identified in bone marrow aspirates. He was noticed to have features of peripheral neuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS syndrome). This is a very rare case of WM with POEMS syndrome which responded to chemotherapy using bortezomib, steroids, and rituximab.http://dx.doi.org/10.1155/2013/890864 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
S. Haider T. Latif A. Hochhausler F. Lucas N. Abdel Karim |
spellingShingle |
S. Haider T. Latif A. Hochhausler F. Lucas N. Abdel Karim Waldenstrom’s Macroglobulinemia and Peripheral Neuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes with a Bleeding Diathesis and Rash Case Reports in Oncological Medicine |
author_facet |
S. Haider T. Latif A. Hochhausler F. Lucas N. Abdel Karim |
author_sort |
S. Haider |
title |
Waldenstrom’s Macroglobulinemia and Peripheral Neuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes with a Bleeding Diathesis and Rash |
title_short |
Waldenstrom’s Macroglobulinemia and Peripheral Neuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes with a Bleeding Diathesis and Rash |
title_full |
Waldenstrom’s Macroglobulinemia and Peripheral Neuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes with a Bleeding Diathesis and Rash |
title_fullStr |
Waldenstrom’s Macroglobulinemia and Peripheral Neuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes with a Bleeding Diathesis and Rash |
title_full_unstemmed |
Waldenstrom’s Macroglobulinemia and Peripheral Neuropathy, Organomegaly, Endocrinopathy, Monoclonal Gammopathy, and Skin Changes with a Bleeding Diathesis and Rash |
title_sort |
waldenstrom’s macroglobulinemia and peripheral neuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes with a bleeding diathesis and rash |
publisher |
Hindawi Limited |
series |
Case Reports in Oncological Medicine |
issn |
2090-6706 2090-6714 |
publishDate |
2013-01-01 |
description |
We report a case of a 29-year-old male who presented with paraesthesia and skin lesions with excessive bleeding after skin biopsy leading to hematology consultation. He was found to have prolonged partial thromboplastin time (PTT) and monoclonal gammopathy on serum protein electrophoresis (SPEP). He experienced excessive bleeding leading to hospitalization after bone marrow biopsy and required blood transfusion. He was diagnosed with Waldenstrom's Macroglobulinemia (WM), based on the presence of IgM-κ type monoclonal (M) protein and infiltration of lymphoplasmacytic cells identified in bone marrow aspirates. He was noticed to have features of peripheral neuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS syndrome). This is a very rare case of WM with POEMS syndrome which responded to chemotherapy using bortezomib, steroids, and rituximab. |
url |
http://dx.doi.org/10.1155/2013/890864 |
work_keys_str_mv |
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