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285 results on '"Hui, Xuhui"'

36. Biodegradable polyurethane-incorporating decellularized spinal cord matrix scaffolds enhance Schwann cell reprogramming to promote peripheral nerve repair

Author

Wang, Yanchao, primary, Lin, Jingjing, additional, Chen, Jinlin, additional, Liang, Ruichao, additional, Zhang, Qiao, additional, Li, Jiehua, additional, Shi, Min, additional, Li, Lei, additional, He, Xueling, additional, Lan, Ting, additional, Hui, Xuhui, additional, and Tan, Hong, additional

Published
2023
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47. Craniopharyngioma with brainstem parenchyma involvement: a rare occurrence.

Author

Deng, Xueyun, He, Shuai, Li, Jiuhong, Ke, Daibo, and Hui, Xuhui

Subjects
CRANIOPHARYNGIOMA, BRAIN stem, INTRACRANIAL tumors, BENIGN tumors
Abstract

This article reports on a rare case of ectopic recurrent craniopharyngioma with brainstem involvement. The patient, a 47-year-old man, experienced visual impairment, limb numbness, and weakness. The tumor divided the brainstem into two parts entirely and filled the fourth ventricle. The patient underwent surgery to remove the tumor, but unfortunately developed a cystic recurrence and passed away six months later. The article emphasizes the importance of regular follow-up after surgery and highlights the challenges of dealing with craniopharyngiomas that invade the brainstem. [Extracted from the article]

Published
2023
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48. Multifocal Desmoplastic Infantile Ganglioglioma/Astrocytoma (DIA/DIG): An Institutional Series Report and a Clinical Summary of This Rare Tumor

Author

Wang, Qiguang, Meng, Jinli, Cheng, Jian, Zhang, Si, Hui, Xuhui, Li, Qiang, Liu, Wenke, Ju, Yan, and Sun, Lin

Subjects
Cancer Research, Oncology
Abstract

AimMultifocal desmoplastic infantile ganglioglioma/astrocytoma (DIA/DIG) has rarely been reported. Here, two cases have been presented, reviewing the literature and proposed treatment algorithms for this rare tumor.Patients and MethodsWe report two patients diagnosed with multifocal DIA/DIGs in West China Hospital. In addition, a literature review was performed, in October 2019, on case reports of DIA/DIGs with multifocal lesions. The clinical and radiological features, treatment, and outcome of this rare disease were discussed.ResultsDIA/DIGs with multifocal locations were rare, and only thirteen cases (including ours) had been reported. This series included 8 males and 5 females with a mean age of 31.4 ± 45.7 months (range, 3-144 months). The supratentorial hemisphere, suprasellar region, posterior cranial fossa, and spinal cord were frequently involved. Ten patients (76.9%) received surgical resection for the symptomatic lesions and three patients (23.1%) underwent biopsy. Seven patients received chemotherapy postoperatively. Six individuals had tumor recurrences during the follow-up period, while three patients had tumors that spontaneously regressed. Finally, two patients died of tumor progression and one patient died of respiratory insufficiency and hypothalamic dysfunction.ConclusionsMultifocal DIA/DIGs have more aggressive clinical behavior and poor outcome despite benign histology. DIA/DIGs should be included in the differential diagnosis of multifocal brain tumors in children. The mainstay of treatment is surgical resection; adjuvant treatment with chemotherapeutic drugs is unknown and requires additional research.

Published
2022

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