2009
DOI: 10.4103/0028-3886.51294
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Cerebellar liponeurocytoma: An updated follow-up of a case presenting histopathological and clinically aggressive features

Abstract: Cerebellar liponeurocytoma is a rare tumor recently included by World Health Organization in the classification of brain tumors as a separate clinicopathological entity separate from medulloblastoma. However, because of the rarity of the tumor, the natural history of the tumor is still not yet been defined. We report a patient with cerebellar liponeurocytoma with unusual clinical and pathological aggressive features. This patient suggests the possible existence of different histological grades of liponeurocyto… Show more

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Cited by 16 publications
(13 citation statements)
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“…10 Recurrent tumors may display increased mitotic activity, increased proliferative activity as assessed by MIB-1 staining, vascular proliferation, and necrosis. [18][19][20] However, some tumors recur in the absence of such atypical histopathologic features. 21,22 It remains to be seen whether these atypical features are truly predictive of more aggressive biologic behavior.…”
Section: Prognosismentioning
confidence: 99%
“…10 Recurrent tumors may display increased mitotic activity, increased proliferative activity as assessed by MIB-1 staining, vascular proliferation, and necrosis. [18][19][20] However, some tumors recur in the absence of such atypical histopathologic features. 21,22 It remains to be seen whether these atypical features are truly predictive of more aggressive biologic behavior.…”
Section: Prognosismentioning
confidence: 99%
“…В доступной нам литературе [11] было найде-но сообщение о метастазировании церебеллярной липонейроцитомы [11], однако ссылок на первич-но-множественный процесс найдено не было. Име-ется описание агрессивного поведения опухоли с инвазией в оболочки мозга и морфологическими признаками малигнизации в виде высокого проли-феративного индекса и клеточной атипии [12].…”
Section: Discussionunclassified
“…Typically, the proliferation index measured with Ki67 is usually low, ranging between 1 and 6%. To date only a few cases of CLNC with atypical histological features comprising prominent microvascular proliferation and/or necrosis have been reported [6,8,24,27]. These cases also presented a high proliferation index and areas of hemorrhages.…”
Section: Discussionmentioning
confidence: 99%
“…Two years after resection, the patient is free of symptoms and radiologic recurrence. Nearly half of patients with cerebellar liponeurocytomas suffer recurrences [20], and a few cases have been reported as clinically aggressive [16,24]. The basic therapeutic method in the described tumor is total neurosurgical resection.…”
Section: Discussionmentioning
confidence: 99%
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