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以发育倒退为表现的毛黏液样星形细胞瘤:一例报告

Pilomyxoid Astrocytoma Presenting With Developmental Regression: A Case Report.

作者信息

Avuthu Om Prasanth Reddy, Salunkhe Shradha, Patil Manojkumar G, C Buch Archana, Mane Shailaja V, Chugh Ashish

机构信息

Paediatrics, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.

Pathology, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.

出版信息

Cureus. 2024 Aug 19;16(8):e67167. doi: 10.7759/cureus.67167. eCollection 2024 Aug.

Abstract

Pilomyxoid astrocytoma (PMA) is a subtype of pilocytic astrocytoma (PA). PMA tends to exhibit a more aggressive course compared to PA. We present a case of a two-year-old male with a PMA in the suprasellar region who presented with developmental regression, loss of previously attained milestones such as the ability to hold his neck, walk, and talk, along with hypotonia in all four limbs. Serum cortisol and thyroid-stimulating hormone (TSH) levels were measured to rule out endocrine disturbances and were within normal limits. Magnetic resonance imaging (MRI) of the brain showed a solid lesion in the suprasellar region, extending into the pituitary and interpeduncular fossae, compressing the pituitary gland, and effacing the third ventricle, causing cerebrospinal fluid (CSF) flow obstruction and lateral ventricle dilation. The tumor appears hypointense on T1 and hyperintense on T2, with fluid-attenuated inversion recovery (FLAIR), peripheral contrast enhancement, and no calcification, consistent with PMA. The CSF analysis was negative for malignant cells. Histopathological examination revealed monomorphous bipolar and spindle cells in an angiocentric pattern with a myxoid background, without rosenthal fibers, mitoses, or eosinophilic granular bodies, consistent with PMA but not seen in PA. Immunohistochemistry showed strong positivity for glial fibrillary acidic protein (GFAP) and S100, with a Ki-67 index of 3-4%, indicating a low-grade tumor. The preferred treatment is surgical resection, but due to the tumor's deep location and potential long-term neurological effects, the parents opted against surgery. A ventriculoperitoneal shunt was placed to alleviate CSF flow, following which the child showed mild improvement in symptoms. Treatment of nonresectable astrocytomas was controversial, but gross total surgical resection offers better disease control. Chemotherapy is for patients with recurrence or where total resection of the tumor is not possible, and radiotherapy, though the long-term disease control is good, has a variable visual outcome.

摘要

毛黏液样星形细胞瘤(PMA)是毛细胞型星形细胞瘤(PA)的一种亚型。与PA相比,PMA往往表现出更具侵袭性的病程。我们报告一例两岁男性,其鞍上区域患有PMA,表现为发育倒退,丧失了之前已达到的里程碑,如抬头、走路和说话的能力,同时四肢肌张力减退。检测血清皮质醇和促甲状腺激素(TSH)水平以排除内分泌紊乱,结果均在正常范围内。脑部磁共振成像(MRI)显示鞍上区域有一个实性病变,延伸至垂体和脚间窝,压迫垂体,使第三脑室消失,导致脑脊液(CSF)流动受阻和侧脑室扩张。肿瘤在T1加权像上呈低信号,在T2加权像上呈高信号,液体衰减反转恢复序列(FLAIR)显示周边强化,无钙化,符合PMA表现。脑脊液分析未发现恶性细胞。组织病理学检查显示以血管为中心的模式中有单形性双极和梭形细胞,伴有黏液样背景,无罗森塔尔纤维、有丝分裂或嗜酸性颗粒体,符合PMA表现,而PA中未见。免疫组化显示胶质纤维酸性蛋白(GFAP)和S100呈强阳性,Ki-67指数为3 - 4%,表明为低级别肿瘤。首选治疗方法是手术切除,但由于肿瘤位置较深且可能产生长期神经学影响,患儿父母选择不进行手术。放置了脑室腹腔分流术以缓解脑脊液流动,之后患儿症状有轻度改善。不可切除星形细胞瘤的治疗存在争议,但肉眼下全切手术能更好地控制疾病。化疗适用于复发患者或无法完全切除肿瘤的患者,放疗虽然长期疾病控制效果良好,但视力预后不一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c31/11408975/ad6c4143f165/cureus-0016-00000067167-i01.jpg

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