1991
DOI: 10.1007/bf01666831
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Intracranial germ cell tumor mimicking anorexia nervosa

Abstract: A previously healthy seventeen-year-old boy developed loss of weight, poor appetite, and aversion to food. Physical examination being normal, anorexia nervosa was suspected. Thirteen months later a CT scan revealed a mass in the third ventricle histologically proven to be a malignant teratoma. To our knowledge anorexia nervosa is only extremely rarely the presenting feature of intracranial germ cell tumors.

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Cited by 10 publications
(3 citation statements)
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“…Attention should also be focused on "atypical" psychiatric features. For instance, a large proportion of the reported cases of anorexia nervosa in patients with brain tumors lacked the evidence of "typical" anorectic behavior toward self-starvation [60][61][62]. The diagnosis of anorexia nervosa in our literature cases was based on criteria such as eating very small quantities of food, fear of becoming obese or retarded puberty and growth [60,63,64].…”
Section: Which Symptoms and Signs Must Raise Suspicion About A Possib...mentioning
confidence: 90%
“…Attention should also be focused on "atypical" psychiatric features. For instance, a large proportion of the reported cases of anorexia nervosa in patients with brain tumors lacked the evidence of "typical" anorectic behavior toward self-starvation [60][61][62]. The diagnosis of anorexia nervosa in our literature cases was based on criteria such as eating very small quantities of food, fear of becoming obese or retarded puberty and growth [60,63,64].…”
Section: Which Symptoms and Signs Must Raise Suspicion About A Possib...mentioning
confidence: 90%
“…To the best of our knowledge this is probably the first case of malignant mixed ICGCT with extra cranial spread presenting as a mass around the right ear in an infant to be reported. Malignant ICGCT is predominantly a tumour of adolescents and young adults, 5,9,10,11,12,13,14,15 although its occurrence in younger children have also been reported. 3,16,17 In infants these tumours are rare and review of available literature revealed a case of congenital mixed malignant ICGCT in a 27 weeks old male fetus involving brain and orbit.…”
Section: Discussionmentioning
confidence: 99%
“…Extra neural metastasis of primary intracranial nongerminomatous GCT to the lung in a 14-year-old girl have been reported. 10 Diagnosis of the condition depends mainly on imaging studies followed by a histological study of the specimen. The main modality of treatment is surgery followed by combination chemotherapy with or without radiation therapy.…”
Section: Discussionmentioning
confidence: 99%