Sella Bugged! Abscess Inside a Craniopharyngioma: Case Report with Literature Review

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY Pediatric Neurosurgery Pub Date : 2022-03-09 DOI:10.1159/000523977
G. Tyagi, Santhosh Kumar S A, Sandeep Kandregula, Radhika Mhatre, A. Uppar
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Abstract

Introduction: Abscess within a craniopharyngioma (CPG) is extremely rare and only 8 such cases have been reported in literature. Most patients present with hypopituitarism and visual disturbances. We report the first ever case of a CPG with abscess in a pediatric patient. Case Report: A 10-year-old girl presented with visual deterioration and bitemporal hemianopia. Her CT and MRI brain suggested of a sellar-suprasellar CPG. Due to ill-developed sino-nasal anatomy, a transcranial approach was made for the lesion. The lesion was well capsulated, thick walled, and appeared inflamed. Upon incising the wall, thick yellowish pus was drained out in a controlled manner. This was followed by a partial resection of the CPG wall and eccentric, adhered, calcified residue was left behind with an Ommaya drain. The abscess culture grew Enterococcus species and histopathology revealed adamantinomatous CPG. Patient underwent culture sensitive antibiotics course followed by radiation for the residue. She was doing well at 1-year follow-up with clinical and radiological improvement. Conclusion: This is the first report of a pediatric case with secondary abscess in CPG. Operative management of such a case includes controlled drainage of pus without dissemination into the surrounding arachnoid space. The tumor and abscess have to be addressed as separate surgical entities; infection control and wherever complete resection is not feasible, partial safe resection followed by radiotherapy is a viable option.
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Sella Bugged!颅咽管瘤内脓肿1例报告并文献复习
引言:颅咽管瘤内脓肿极为罕见,文献中仅报道了8例此类病例。大多数患者表现为垂体功能减退和视觉障碍。我们报告了有史以来第一例CPG并发脓肿的儿科患者。病例报告:一名10岁女孩出现视力下降和双颞侧偏盲。她的CT和MRI大脑显示为鞍上CPG。由于鼻窦解剖结构发育不良,对病变进行了经颅入路治疗。病变包膜良好,壁厚,出现炎症。切开壁后,粘稠的黄色脓液以可控的方式排出。随后对CPG壁进行了部分切除,并用Ommaya引流管留下了偏心、粘附、钙化的残留物。脓肿培养生长出肠球菌种,组织病理学显示为造釉细胞性CPG。患者接受了对培养敏感的抗生素疗程,随后对残留物进行了放射治疗。她在一年的随访中表现良好,临床和放射学有所改善。结论:这是第一例CPG继发脓肿的儿科病例报告。这种病例的手术治疗包括控制脓液的排出,而不扩散到周围的蛛网膜间隙。肿瘤和脓肿必须作为单独的外科实体来处理;感染控制,在完全切除不可行的地方,部分安全切除后放疗是可行的选择。
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来源期刊
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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