Granular cell tumour
نویسندگان
چکیده
منابع مشابه
Granular cell tumour (Abrikossoff’s tumour): Case series
This case series describes three unreported cases of an uncommon benign neoplasm named Abrikossoff’s tumour or granular cell tumour (GCT). This mesenchymal neoplasm apparently arises from neural or Schwann cell origin with benign and malignant forms. All cases presented here were unique nodules on oral mucosa, coming out from the connective tissue, and occurring in women with age ranging from 3...
متن کاملGranular cell tumour: a rare caruncle lesion.
1 Zimmerman LE. Phakomatous choristoma of the eyelid. A tumor of lenticular anlage. Am J Ophthalmol 1971;1(Part 2):169–77. 2 Shin HM, Song HG, Choi MY. Phakomatous choristoma of the eyelid. Korean J Ophthalmol 1999;13:133–7. 3 Sinclair-Smith CC, Emms M, Morris HB. Phakomatous choristoma of the lower eyelid. A light and ultrastructural study. Arch Pathol Lab Med 1989;113:1175–7. 4 Ellis FJ, Eagl...
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With only 16 cases reported in the literature, the mostly benign granular cell tumour of the urinary bladder is exceptionally rare. We present the case of a 68-year old patient with one of these lesions demonstrating our histological findings including several immunohistochemical stainings used to differentiate between other more common entities.
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Granular cell tumor is a rare neoplasm that may involve the larynx. It is almost always benign. Laryngologists should be familiar with this unusual tumor, its implications and appropriate treatment.
متن کاملMalignant granular cell tumour of the mediastinum.
This report describes a case of malignant granular cell tumour arising in the mediastinum, detailing the investigations undertaken to reach this rare diagnosis. A 63-year-old man was referred from the Pacific Islands for investigation of a 8cm mediastinal mass extending into the left pleura and associated with pleural nodules and pleural effusion. Needle aspiration via bronchoscopy yielded insu...
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ژورنال
عنوان ژورنال: Journal of Cutaneous and Aesthetic Surgery
سال: 2015
ISSN: 0974-2077
DOI: 10.4103/0974-2077.167288