Kantar Mehmet, Sezak Murat, Turhan Tuncer, Kitis Omer, Mutluer Saffet, Demirag Bengu K, Aksoylar Serap, Akalin Taner, Ersahin Yusuf, Cetingul Nazan
Pediatric Oncology Unit, Department of Pediatrics, Ege University School of Medicine, 35100, Izmir, Turkey.
Childs Nerv Syst. 2008 Nov;24(11):1371-5. doi: 10.1007/s00381-008-0664-y. Epub 2008 Jul 1.
Melanotic progonoma or melanotic neuroectodermal tumor is a rare tumor in infancy. This lesion has to be considered in the differential diagnosis of benign or malignant lesions of calvarium.
The authors present a case of a 4-month-old infant with left retroauricular mass. The patient had a subcutaneous mass that is fixed to the underlying skull. CT and MRI scans showed left occipitotemporal expansile mass. The tumor was removed by surgery. A tumor, brownish-black in color, was diagnosed as melanotic progonoma. The patient remained symptom-free for the last 2 years after complete surgery.
Extracranial subcutaneous masses involving the skull are uncommon in infants. Benign or malignant lesions may occur as lumps on calvarium. Physical examination and some laboratory findings are helpful in the assessment of patient. Benign or malignant lesions can be differentiated by craniography, CT, or MRI scans, but exact diagnosis of melanotic progonoma is made by histopathology and immunostaining, as was in the presented case. Cranial vault progonomas have a better outcome by complete surgery. The tumors usually do not recur in long-term period.
黑素性促性腺瘤或黑素性神经外胚层肿瘤是婴儿期罕见的肿瘤。在鉴别诊断颅骨的良性或恶性病变时必须考虑到这种病变。
作者报告1例4个月大的婴儿,其左耳后有肿块。患者有一个皮下肿块,与下方颅骨相连。CT和MRI扫描显示左枕颞叶有膨胀性肿块。通过手术切除肿瘤。一个棕黑色的肿瘤被诊断为黑素性促性腺瘤。在完全手术后的过去2年里,患者一直无症状。
婴儿期累及颅骨的颅外皮下肿块并不常见。良性或恶性病变可能表现为颅骨上的肿块。体格检查和一些实验室检查结果有助于评估患者。良性或恶性病变可通过颅骨造影、CT或MRI扫描进行鉴别,但黑素性促性腺瘤的准确诊断需通过组织病理学和免疫染色,本病例即是如此。通过完全手术,颅顶促性腺瘤的预后较好。这些肿瘤通常长期不会复发。