scholarly journals Anti-Ri-Associated Paraneoplastic Neurological Syndrome Revealing Breast Cancer: A Case Report

Cureus ◽  
2022 ◽  
Author(s):  
Rim Tazi ◽  
Zakaria Salimi ◽  
Hajar Fadili ◽  
Jehanne Aasfara ◽  
Asmaa Hazim
Breast Cancer ◽  
2006 ◽  
Vol 13 (2) ◽  
pp. 202-204 ◽  
Author(s):  
Teru Kawasoe ◽  
Yutaka Yamamoto ◽  
Yasuhiro Okumura ◽  
Hirotaka Iwase

2003 ◽  
Vol 269 (1) ◽  
pp. 62-65 ◽  
Author(s):  
C. Dorn ◽  
C. Knobloch ◽  
M. Kupka ◽  
N. Morakkabati-Spitz ◽  
J. Schmolling

2018 ◽  
Vol 25 (6) ◽  
pp. 1526-1530 ◽  
Author(s):  
Omer Fatih Olmez ◽  
Oguzcan Kinikoglu ◽  
Nesrin Helvacı Yilmaz ◽  
Ahmet Bilici ◽  
Erdem Cubukcu ◽  
...  

Paraneoplastic neurological syndrome is associated with anti-Ri antibodies, which are typically present with opsoclonus–myoclonus–ataxia. Human epidermal growth factor receptor 2 (HER2) overexpression is present in 15%–25% of breast cancer and is associated with poor prognosis. There are a few reports of paraneoplastic neurological syndrome associated with HER2-positive breast cancer in the literature, of which most are anti-Yo-associated paraneoplastic neurological syndrome. We present herein the case of a female patient with HER2-positive breast cancer who had atypical anti-Ri antibody associated with opsoclonus–myoclonus paraneoplastic neurological syndrome. Following the diagnosis of paraneoplastic syndrome, chemotherapy with dual HER2 blockade and immunomodulating treatment including intravenous immunoglobulin and oral prednisolone were administered. Although the patient was negative for serum anti-Ri antibodies, there was partial clinical improvement and her neurological deficit persisted. To our knowledge, this is the first case report of female patient with HER2-positive breast cancer who had atypical anti-Ri antibody associated with opsoclonus–myoclonus paraneoplastic neurological syndrome and treated with dual HER2 blockade.


2019 ◽  
Vol 48 (2) ◽  
pp. 030006051987174
Author(s):  
Yuyao Wang ◽  
Yang Bian ◽  
Feng Qiu ◽  
Pu Fang

Paroxysmal vertigo as the presenting symptom of a fallopian tube tumor is rare among patients. We present a patient who was finally diagnosed with fallopian tube serous adenocarcinoma with subacute cerebellar degeneration. We analyzed the patients’ clinical, pathological, and imaging data. We conclude that the possibility of paraneoplastic neurological syndrome should be considered when conventional treatment is ineffective for a fallopian tube tumor and other neurological diseases are excluded.


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