Granular cell tumor: a clinicopathologic study of 110 patients
| Autor: | Byungkyu Chun, Callihan, G F Worsham, S Klappenbach, B E Crawford, Ernest E. Lack, G Rowden |
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| Rok vydání: | 1980 |
| Předmět: |
Adult
Male Pathology medicine.medical_specialty Skin Neoplasms Pseudoepitheliomatous Hyperplasia Epidermal Cyst Fibroma Diagnosis Differential Neoplasms Muscle Tissue Sex Factors medicine Carcinoma Malignant Granular Cell Tumor Humans Esophagus Mouth neoplasm Granular cell tumor business.industry Age Factors General Medicine medicine.disease medicine.anatomical_structure Oncology Esophageal Granular Cell Tumor Surgery Female Mouth Neoplasms business Adenofibroma |
| Zdroj: | Journal of surgical oncology. 13(4) |
| ISSN: | 0022-4790 |
| Popis: | The clinicopathologic features of 118 granular cell tumors (GCT) encountered at two affiliated hospitals were reviewed. A total of 110 patients were affected over this 32-year period of study (71 men, 39 women), and in 5% GCT were multiple. Patients ranged in age from 16 to 58 years (average 32 years) and were symptomatic for an average duration of 11 months prior to diagnosis. There was a greater than expected frequency of GCT among black patients (29%). Although tongue was the single most common anatomic site involved, relatively more GCT (44%) occurred in skin or subcutaneous tissue. Less common locations were breast parenchyma (10 cases), rectal mucosa and anus (6), vulva (4), esophagus and larynx (2 cases each). The correct preoperative diagnosis of this protean tumor was made in only three patients. GCT were surgically treated with the average diameter of resected tumor being 1.2 cm (range 0.2--3.5 cm). Pseudoepitheliomatous hyperplasia was noted in 11 tumors and in one vulvar GCT there was overlying in situ squamous cell carcinoma. Tumors were incompletely excised in 24 of 56 patients having adequate followup; only five of these 24 patients experienced a local recurrence of tumor. Malignant behavior was not observed. Results of histochemical and ultrastructural study are briefly discussed. The precise histogenesis of GCT is uncertain but Schwann cell origin is favored in most cases. |
| Databáze: | OpenAIRE |
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