Granular cell tumor in the scrotum of a pediatric patient: A case report of a rare clinical entity

被引:0
作者
Ashbrook, Caleb [1 ,4 ]
Batie, Shane F. [1 ,2 ]
Sengupta, Anita [1 ,3 ]
Peters, Craig A. [1 ,2 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Urol, 2001 Inwood Rd,4th Floor,West Campus Bldg, Dallas, TX 75390 USA
[2] Childrens Med Ctr, Dept Urol, 2350 N Stemmons Freeway F4300, Dallas, TX 75207 USA
[3] Childrens Med Ctr, Dept Pathol, C1529,1935 Med Dist Dr, Dallas, TX 75235 USA
[4] Inwood Rd, 4th Floor, West Campus Bldg, Dallas, TX 75390 USA
来源
UROLOGY CASE REPORTS | 2023年 / 47卷
关键词
Granular cell tumor; Scrotum; Pediatrics;
D O I
10.1016/j.eucr.2023.102327
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Granular cell tumors are rare tumors of Schwann cell origin that present in any anatomic location, age or sex. We present a case of a granular cell tumor in the scrotum of a prepubescent male. The tumor was excised, with histology revealing abundant eosinophilic cytoplasm and positive S-100 staining. No stigmata of malignancy were identified and no recurrence has been reported during follow-up.
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页数:3
相关论文
共 5 条
[1]   Malignant granular cell tumor of soft tissue - Diagnostic criteria and clinicopathologic correlation [J].
Fanburg-Smith, JC ;
Meis-Kindblom, JM ;
Fante, R ;
Kindblom, LG .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1998, 22 (07) :779-794
[2]   Granular cell tumor a study of 42 cases and systemic review of the literature [J].
Mobarki, Mousa ;
Dumollard, Jean Marc ;
Dal Col, Pierre ;
Camy, Florian ;
Peoc'h, Michel ;
Karpathiou, Georgia .
PATHOLOGY RESEARCH AND PRACTICE, 2020, 216 (04)
[3]  
Neelon D, 2022, STATPEARLS
[4]   Granular cell tumor presenting in the scrotum of a pediatric patient: A case report and review of the literature [J].
Richmond A.M. ;
La Rosa F.G. ;
Said S. .
Journal of Medical Case Reports, 10 (1)
[5]   Multiple granular cell tumors are an associated feature of LEOPARD syndrome caused by mutation in PTPN11 [J].
Schrader, K. A. ;
Nelson, T. N. ;
De Luca, A. ;
Huntsman, D. G. ;
McGillivray, B. C. .
CLINICAL GENETICS, 2009, 75 (02) :185-189