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1.
Cureus ; 16(3): e56434, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38638776

ABSTRACT

Cushing's syndrome is a constellation of features occurring due to high blood cortisol levels. We report a case of a 47-year-old male with a history of recurrent olfactory neuroblastoma (ONB). He presented with bilateral lower limb weakness and anosmia and was found to have Cushing's syndrome due to high adrenocorticotropic hormone (ACTH) levels from an ectopic source, ONB in this case. Serum cortisol and ACTH levels declined after tumor removal.

2.
Neurosciences (Riyadh) ; 26(3): 284-288, 2021 Jul.
Article in English | MEDLINE | ID: mdl-34230084

ABSTRACT

Rosette-forming glioneural tumors (RGNTs) are rare. Here, we report a case of RGNT of the fourth ventricle in an 18-year-old female. The patient presented with a 4-month history of headache and dizziness. Neurological examination showed papilledema, impaired tandem gait, and right-sided dysmetria. Radiological images showed a posterior fossa lesion in the fourth ventricle with hydrocephalus. An emergent ventriculostomy was performed followed by gross total surgical resection of the lesion. Histopathological examination confirmed the diagnosis of RGNT. The patient developed posterior fossa syndrome postoperatively which improved on follow-up. Although rare, RGNT should be considered in the differential diagnoses of posterior fossa lesions in young patients. Given its benign course, surgical resection remains the treatment of choice.


Subject(s)
Cerebral Ventricle Neoplasms , Hydrocephalus , Adolescent , Cerebral Ventricle Neoplasms/complications , Cerebral Ventricle Neoplasms/diagnostic imaging , Cerebral Ventricle Neoplasms/surgery , Diagnosis, Differential , Female , Fourth Ventricle/diagnostic imaging , Fourth Ventricle/surgery , Humans , Hydrocephalus/diagnostic imaging , Hydrocephalus/etiology , Hydrocephalus/surgery , Magnetic Resonance Imaging
3.
J AAPOS ; 20(4): 372-4, 2016 08.
Article in English | MEDLINE | ID: mdl-27373441

ABSTRACT

An 11-year-old girl with Joubert syndrome was evaluated for a dim red reflex in her left eye. Fundus examination revealed retinal telangiectasias bilaterally compatible with Coats-like pigmentary retinopathy, a phenomenon not previously reported in Joubert syndrome. Coats-like exudative retinopathy may result in permanent visual loss if left untreated. The exudative retinopathy was controlled after multiple sessions of indirect laser photocoagulation and cryotherapy, with a good visual outcome.


Subject(s)
Abnormalities, Multiple/diagnosis , Cerebellum/abnormalities , Eye Abnormalities/diagnosis , Kidney Diseases, Cystic/diagnosis , Retina/abnormalities , Retinal Telangiectasis/etiology , Abnormalities, Multiple/pathology , Cerebellum/pathology , Child , Eye Abnormalities/pathology , Female , Humans , Kidney Diseases, Cystic/pathology , Laser Coagulation , Retina/pathology , Retinal Telangiectasis/diagnosis
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