Autoimmune Encephalitis as a Rare Paraneoplastic Syndrome in Adrenocortical Carcinoma
Copyright: © 2023 Indian Journal of Nuclear Medicine..
Paraneoplastic neurologic syndromes (PNSs) are rare in pediatrics and are understood to be consequences of cross-reactivity against various neuroendocrine antigens expressed on cancer cells. Here, we report a case of autoimmune encephalitis, a type of PNS associated with a case of adrenocortical carcinoma (ACC), that had a clinical response to immunosuppressive therapy. ACC is a rare tumor with controversial tissue of origin but expresses various neuroendocrine antigens that could be the possible mechanism for this rare yet interesting association.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:38 |
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Enthalten in: |
Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India - 38(2023), 4 vom: 19. Okt., Seite 376-378 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Mohapatra, Debabrata [VerfasserIn] |
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Links: |
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Themen: |
Adrenocortical carcinoma |
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Anmerkungen: |
Date Revised 24.02.2024 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
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doi: |
10.4103/ijnm.ijnm_26_23 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM368805212 |
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520 | |a Paraneoplastic neurologic syndromes (PNSs) are rare in pediatrics and are understood to be consequences of cross-reactivity against various neuroendocrine antigens expressed on cancer cells. Here, we report a case of autoimmune encephalitis, a type of PNS associated with a case of adrenocortical carcinoma (ACC), that had a clinical response to immunosuppressive therapy. ACC is a rare tumor with controversial tissue of origin but expresses various neuroendocrine antigens that could be the possible mechanism for this rare yet interesting association | ||
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