Literature DB >> 27758720

[Autoimmune encephalitis due to mantle cell lymphoma].

A A H Bressers1, N A Goto, S Piepers, J C Regelink.   

Abstract

BACKGROUND: Autoimmune encephalitis is a rare condition characterized by subacute development of cognitive and psychiatric symptoms. A paraneoplastic syndrome involves autoimmune encephalitis caused by classic antibodies. Although this condition is often associated with cancer, no malignancy has yet been found in 70-90% of patients at the time of diagnosis. CASE DESCRIPTION: We saw a 58-year-old male patient with fatigue, diarrhoea and weight loss. He was also experiencing hyperekplexia, personality changes and an instable gait. PET-CT revealed generalised lymphadenopathy. Histopathological analysis of a lymph node showed mantle cell lymphoma. Further investigation of the fluid revealed anti-DPPX IgG antibodies. We treated the patient's mantle cell lymphoma with R-CHOP; he achieved complete remission and his neurological symptoms resolved almost completely.
CONCLUSION: The presence of anti-DPPX IgG antibodies is rare. Although it has not been proven that these antibodies are related to malignancies, this is the third of 30 known cases in which anti-DPPX IgG antibodies and a lymphatic malignancy were found.

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Year:  2016        PMID: 27758720

Source DB:  PubMed          Journal:  Ned Tijdschr Geneeskd        ISSN: 0028-2162


  2 in total

1.  Dipeptidyl-peptidase-like protein 6 encephalitis treated with immunotherapy.

Authors:  Lan Ye; Margret Schnegelsberg; Mark Obermann
Journal:  Proc (Bayl Univ Med Cent)       Date:  2020-09-28

Review 2.  Typical clinical and imaging manifestations of encephalitis with anti-γ-aminobutyric acid B receptor antibodies: clinical experience and a literature review.

Authors:  Zhihua Si; Aihua Wang; Jinzhi Liu; Zixian Zhang; Ke Hu
Journal:  Neurol Sci       Date:  2019-01-22       Impact factor: 3.307

  2 in total

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