Extratesticular gliomatosis peritonei after mesenteric teratoma: a case report and literature review

被引:5
作者
Li, Jiaqiang [1 ]
Li, Shoulin [1 ]
Xiao, Dong [2 ]
Song, Jiaming [3 ]
Mao, Jianxiong [2 ]
Yin, Jianchun [1 ]
机构
[1] Shenzhen Childrens Hosp, Dept Pediat Urol, 7019 Yitian Rd, Shenzhen 518036, Guangdong, Peoples R China
[2] Shenzhen Childrens Hosp, Dept Pediat Gen Surg, Shenzhen, Guangdong, Peoples R China
[3] Shenzhen Childrens Hosp, Dept Pathol, Shenzhen, Guangdong, Peoples R China
关键词
Mesenteric teratoma; extratesticular gliomatosis peritonei; peritoneum; child; lesion; epididymis; IMMATURE TERATOMA;
D O I
10.1177/03000605211047076
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mesenteric teratoma is a rare extragonadal teratoma. Gliomatosis peritonei (GP) is mature glial tissue implanted into the peritoneum's surface and is mainly accompanied by ovarian teratoma. Only a few cases of gliomatosis have occurred in the extraperitoneum. We present a rare case of a 3-year-old boy who presented with extratesticular GP after excision of an immature mesenteric teratoma at 2 months old. After the extratesticular mass was excised, we found ductile tissue on the surface of the terminal spermatic cord and epididymis. Some ductile tissue of the epididymis was removed and sent to a laboratory for a pathological examination. The mass and the ductile tissue of the epididymis had a hard consistency. The pathological diagnosis was extratesticular gliomatosis. Complete surgical resection of the teratoma and GP is helpful for identifying the presence of malignant lesions and for preventing malignant transformation. However, characteristics of GP lesions are extensive and they are difficult to completely remove. Moreover, GP is usually benign. Therefore, the residual GP tissue was not completely removed in our case. The child is still in good health, but requires lifelong follow-up. In conclusion, we report our experience of a rare case of extraperitoneal GP from an extragonadal teratoma.
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页数:8
相关论文
共 17 条
[1]  
Al-Arfaj AA, 2003, SAUDI MED J, V24, P1388
[2]   PERITONEAL GLIOMATOSIS FROM A GASTRIC TERATOMA [J].
COULSON, WF .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1990, 94 (01) :87-89
[3]  
Dadmanesh F, 1997, MODERN PATHOL, V10, P597
[4]   Glial implants in gliomatosis peritonei arise from normal tissue, not from the associated teratoma [J].
Ferguson, AW ;
Katabuchi, H ;
Ronnett, BM ;
Cho, KR .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 159 (01) :51-55
[5]   Immature ovarian teratoma with unusual gliomatosis [J].
Gheorghisan-Galateanu, Ancuta ;
Terzea, Dana Cristina ;
Carsote, Mara ;
Poiana, Catalina .
JOURNAL OF OVARIAN RESEARCH, 2013, 6
[6]   GLIOMATOSIS PERITONEI IN CHILDHOOD AND ADOLESCENCE - CLINICOPATHOLOGICAL STUDY OF 13 CASES INCLUDING IMMUNOHISTOCHEMICAL FINDINGS [J].
HARMS, D ;
JANIG, U ;
GOBEL, U .
PATHOLOGY RESEARCH AND PRACTICE, 1989, 184 (04) :422-430
[7]   Peritoneal and Nodal Gliomatosis with Endometriosiso Accompanied with Ovarian Immature Teratoma: A Case Study and Literature Review [J].
Kim, Na Rae ;
Lim, Soyi ;
Jeong, Juhyeon ;
Cho, Hyun Yee .
KOREAN JOURNAL OF PATHOLOGY, 2013, 47 (06) :587-591
[8]   Is gliomatosis peritonei derived from the associated ovarian teratoma? [J].
Kwan, MY ;
Kalle, W ;
Lau, GTC ;
Chan, JKC .
HUMAN PATHOLOGY, 2004, 35 (06) :685-688
[9]   Gliomatosis peritonei: a clinicopathologic and immunohistochemical study of 21 cases [J].
Liang, Li ;
Zhang, Yifen ;
Malpica, Anais ;
Ramalingam, Preetha ;
Euscher, Elizabeth D. ;
Fuller, Gregory N. ;
Liu, Jinsong .
MODERN PATHOLOGY, 2015, 28 (12) :1613-1620
[10]   Gliomatosis peritonei associated with a ventriculo-peritoneal shunt [J].
Lobotesis, K. ;
U-King-Im, J. M. ;
Cross, J. J. ;
Gillard, J. H. ;
Antoun, N. M. .
CLINICAL RADIOLOGY, 2009, 64 (01) :95-99