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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Main Authors: Gabriel Cojuc-Konigsberg, Isabel Natera-Comte, Blanca E. López Graciano, Luis Gerardo Mosqueda López, José Alonso Ávila-Rojo, Braulio Martínez, Juan C. Ramírez-Sandoval
Format: Article
Language:English
Published: Hindawi Limited 2022-01-01
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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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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