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DOI 10.1097/cnd.0000000000000099

Медицинская библиотека · Journal of clinical neuromuscular disease · 2015

POEMS Syndrome in a Juvenile Initially Diagnosed as Treatment Resistant Chronic Inflammatory Demyelinating Polyneuropathy.

Krish Sonia N, Nguyen Thy, Biliciler Suur, Kumaravel Manickam, Wahed Amer, Risin Semyon, Sheikh Kazim A

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Аннотация

POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, skin changes) is a disorder that mainly affects adults. We report a pediatric patient, initially considered to have Guillain-Barré syndrome, who continued to have progression of neuropathic disease leading to the diagnosis of chronic inflammatory demyelinating polyneuropathy. Diagnosis of POEMS was established by an abnormal bone marrow biopsy, prompted by laboratory and imaging findings, which became abnormal later in the course of the disease. POEMS syndrome is extremely rare in children, and neuropathic features in this age group have not been previously described. This case illustrates that "Guillain-Barré syndrome-like" initial presentation for POEMS, which has not been previously reported. It also emphasizes that in children with progressive acquired neuropathies that are treatment unresponsive, POEMS syndrome should be considered.

Для цитирования: Krish Sonia N, Nguyen Thy, Biliciler Suur, Kumaravel Manickam, Wahed Amer, Risin Semyon, Sheikh Kazim A. POEMS Syndrome in a Juvenile Initially Diagnosed as Treatment Resistant Chronic Inflammatory Demyelinating Polyneuropathy.. Journal of clinical neuromuscular disease. 2015. DOI: 10.1097/cnd.0000000000000099.

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