A Nonseminomatous Germ Cell Tumor Presenting as a Mixed Cryoglobulinemic Vasculitis
Background. Mixed cryoglobulinemia syndrome (MCS) is a rare entity with a variety of causes but has not been associated with testicular germ cell tumors. We present here a case of a patient with a nonseminomatous germ cell tumor (NSGCT) presenting as a type III mixed cryoglobulinemic vasculitis. Cas...
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Language: | English |
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Hindawi Limited
2022-01-01
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Series: | Case Reports in Oncological Medicine |
Online Access: | http://dx.doi.org/10.1155/2022/3326761 |
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author | Gabriel Cojuc-Konigsberg Isabel Natera-Comte Blanca E. López Graciano Luis Gerardo Mosqueda López José Alonso Ávila-Rojo Braulio Martínez Juan C. Ramírez-Sandoval |
author_facet | Gabriel Cojuc-Konigsberg Isabel Natera-Comte Blanca E. López Graciano Luis Gerardo Mosqueda López José Alonso Ávila-Rojo Braulio Martínez Juan C. Ramírez-Sandoval |
author_sort | Gabriel Cojuc-Konigsberg |
collection | DOAJ |
description | Background. Mixed cryoglobulinemia syndrome (MCS) is a rare entity with a variety of causes but has not been associated with testicular germ cell tumors. We present here a case of a patient with a nonseminomatous germ cell tumor (NSGCT) presenting as a type III mixed cryoglobulinemic vasculitis. Case Presentation. A 58-year-old male exhibited typical clinical features of vasculitis, including weakness, fatigue, palpable purpura, multiple mononeuropathy, and a low C4 level. An MCS diagnosis was confirmed by the presence of cryoglobulins (6%) with polyclonal IgM and IgG components and biopsy proven leukocytoclastic vasculitis. Concomitantly, a stage IIIC (TxNxM1bS1) germ tumor with marked elevation of serum beta-human chorionic gonadotropin (2764 mUI/mL) was diagnosed. An aggressive treatment was needed, including methylprednisolone pulses, plasmapheresis, rituximab, followed by orchiectomy, and chemotherapy (bleomycin/etoposide/cisplatin). After tumor resection and treatment, cryoglobulins decrease to 0%, suggesting a paraneoplastic origin of the vasculitis. Conclusion. To the best of our knowledge, this is the first case of MCS possibly attributable to a NSGCT. This case further elaborates on the presentation of mixed cryoglobulinemia vasculitis and adds to the published literature on the topic. |
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language | English |
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publishDate | 2022-01-01 |
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series | Case Reports in Oncological Medicine |
spelling | doaj.art-69dee1c8950940d98262bffb7335b4da2023-05-06T00:00:01ZengHindawi LimitedCase Reports in Oncological Medicine2090-67142022-01-01202210.1155/2022/3326761A Nonseminomatous Germ Cell Tumor Presenting as a Mixed Cryoglobulinemic VasculitisGabriel Cojuc-Konigsberg0Isabel Natera-Comte1Blanca E. López Graciano2Luis Gerardo Mosqueda López3José Alonso Ávila-Rojo4Braulio Martínez5Juan C. Ramírez-Sandoval6Instituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránInstituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránInstituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránInstituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránInstituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránInstituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránInstituto Nacional de Ciencias Médicas y Nutrición Salvador ZubiránBackground. Mixed cryoglobulinemia syndrome (MCS) is a rare entity with a variety of causes but has not been associated with testicular germ cell tumors. We present here a case of a patient with a nonseminomatous germ cell tumor (NSGCT) presenting as a type III mixed cryoglobulinemic vasculitis. Case Presentation. A 58-year-old male exhibited typical clinical features of vasculitis, including weakness, fatigue, palpable purpura, multiple mononeuropathy, and a low C4 level. An MCS diagnosis was confirmed by the presence of cryoglobulins (6%) with polyclonal IgM and IgG components and biopsy proven leukocytoclastic vasculitis. Concomitantly, a stage IIIC (TxNxM1bS1) germ tumor with marked elevation of serum beta-human chorionic gonadotropin (2764 mUI/mL) was diagnosed. An aggressive treatment was needed, including methylprednisolone pulses, plasmapheresis, rituximab, followed by orchiectomy, and chemotherapy (bleomycin/etoposide/cisplatin). After tumor resection and treatment, cryoglobulins decrease to 0%, suggesting a paraneoplastic origin of the vasculitis. Conclusion. To the best of our knowledge, this is the first case of MCS possibly attributable to a NSGCT. This case further elaborates on the presentation of mixed cryoglobulinemia vasculitis and adds to the published literature on the topic.http://dx.doi.org/10.1155/2022/3326761 |
spellingShingle | Gabriel Cojuc-Konigsberg Isabel Natera-Comte Blanca E. López Graciano Luis Gerardo Mosqueda López José Alonso Ávila-Rojo Braulio Martínez Juan C. Ramírez-Sandoval A Nonseminomatous Germ Cell Tumor Presenting as a Mixed Cryoglobulinemic Vasculitis Case Reports in Oncological Medicine |
title | A Nonseminomatous Germ Cell Tumor Presenting as a Mixed Cryoglobulinemic Vasculitis |
title_full | A Nonseminomatous Germ Cell Tumor Presenting as a Mixed Cryoglobulinemic Vasculitis |
title_fullStr | A Nonseminomatous Germ Cell Tumor Presenting as a Mixed Cryoglobulinemic Vasculitis |
title_full_unstemmed | A Nonseminomatous Germ Cell Tumor Presenting as a Mixed Cryoglobulinemic Vasculitis |
title_short | A Nonseminomatous Germ Cell Tumor Presenting as a Mixed Cryoglobulinemic Vasculitis |
title_sort | nonseminomatous germ cell tumor presenting as a mixed cryoglobulinemic vasculitis |
url | http://dx.doi.org/10.1155/2022/3326761 |
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