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Tubulointerstitial nephritis with IgA kappa-positive plasma cells in a patient with primary Sjögren's syndrome and monoclonal gammopathy.
Sonomura, Kazuhiro; Oobayashi, Yuuki; Iimori, Misa; Yamauchi, Hiroko; Nakayama, Mayuka.
Afiliación
  • Sonomura K; Department of Nephrology, Japanese Red Cross Society Kyoto Daiichi Hospital, 15-749 Honmachi Higashiyamaku Kyoto-Shi, Kyoto, 606-0981, Japan. sono0823@koto.kpu-m.ac.jp.
  • Oobayashi Y; Department of Nephrology, Japanese Red Cross Society Kyoto Daiichi Hospital, 15-749 Honmachi Higashiyamaku Kyoto-Shi, Kyoto, 606-0981, Japan.
  • Iimori M; Department of Nephrology, Japanese Red Cross Society Kyoto Daiichi Hospital, 15-749 Honmachi Higashiyamaku Kyoto-Shi, Kyoto, 606-0981, Japan.
  • Yamauchi H; Department of Nephrology, Japanese Red Cross Society Kyoto Daiichi Hospital, 15-749 Honmachi Higashiyamaku Kyoto-Shi, Kyoto, 606-0981, Japan.
  • Nakayama M; Department of Nephrology, Japanese Red Cross Society Kyoto Daiichi Hospital, 15-749 Honmachi Higashiyamaku Kyoto-Shi, Kyoto, 606-0981, Japan.
CEN Case Rep ; 12(2): 200-204, 2023 05.
Article en En | MEDLINE | ID: mdl-36367665
This is a case report of a 69-year-old Japanese man who has been undergoing treatment for primary Sjögren's syndrome (pSS) since he was 62 years. A renal biopsy, which revealed diffuse and severe mononuclear cell infiltration in the tubulointerstitium, was performed because of progressive renal dysfunction. Immunostaining demonstrated most of the infiltrating cells to be IgA, kappa, CD38, and CD138 positive. Immunofixation blood test revealed IgA kappa-type M protein; however, bone marrow abnormalities or lymph node enlargements on examination or imaging, respectively, were not observed. Tubulointerstitial nephritis caused by monotypic plasmacytic infiltration in pSS, accompanied with a monoclonal gammopathy of undetermined significance (MGUS), was diagnosed. A treatment of prednisolone 40 mg/day was initiated, promptly improving the patient's serum creatinine levels from 3.0 to 1.5 mg/dl. The infiltrating cells in pSS-associated tubulointerstitial nephritis are generally polytypic plasmacytes and lymphocytes, but in the present case, monotypic plasmacytes were predominant. This case is remarkable and rare and can be considered a complication of pSS or MGUS. Since it may become a new disease entity, it is important to accumulate similar cases.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraproteinemias / Gammopatía Monoclonal de Relevancia Indeterminada / Síndrome de Sjögren / Nefritis Intersticial Límite: Aged / Humans / Male Idioma: En Revista: CEN Case Rep Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Paraproteinemias / Gammopatía Monoclonal de Relevancia Indeterminada / Síndrome de Sjögren / Nefritis Intersticial Límite: Aged / Humans / Male Idioma: En Revista: CEN Case Rep Año: 2023 Tipo del documento: Article País de afiliación: Japón