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Case Report
A case of paraneoplastic limbic encephalitis due to ovarian mature teratoma
Seong Heon Kim, hye Young Kim, Young Tak Im, Sang Ook Nam, Young Mi Kim
Clin Exp Pediatr. 2010;53(4):603-606.   Published online April 15, 2010
Paraneoplastic limbic encephalitis, a remote effect of cancer without nervous system metastasis, is rare, especially in childhood. Here, we report a case of paraneoplastic limbic encephalitis associated with an ovarian mature teratoma in an adolescent girl. The 15-year-old girl developed neuropsychiatric symptoms, memory loss, seizures, and unconsciousness. Cerebrospinal fluid analysis and brain magnetic resonance imaging (MRI) findings were normal, while...
One Case of Maffucco's Syndrome with Testicular Teratoma
Seung Mo Park, Duk Hi Kim, Ho Seong Kim
Clin Exp Pediatr. 1994;37(8):1162-1168.   Published online August 15, 1994
Maffucci's syndrome is a very rare, congenital and non-hereditary mesodermal dysplasia manifested by multiple enchondromas and soft tissue hemangiomas. Since Maffucci had reported this syndrome in 1881, there have been more than 100 cases reported, and also there has been reported that Maffuddi's syndrome has various interstitial tumor. However there hasn't been any report about Maffucci's syndrome with testicular teratoma....
A Case of Nasopharyngeal Teratoma Showing Upper Airway Obstruction
Jeong Ho Jeon, In Seok Lim, Chul Hwa Kim, Byeng Hoon Yoo
Clin Exp Pediatr. 1994;37(4):560-564.   Published online April 15, 1994
Neoplasms of the nasophrynx are rare in neonates and infants. The most common nasopharyngeal tumor encountered in this age group is teratoma-neoplasm containing multiple heterotopic tissues. Four histologic types of nasopharyngeal teratoma occur-dermoid, teratoid, true teratoma, epignathing of which dermoid is most frequently seen. We have experienced a case of nasopharyngeal teratoma in a female neonate with signs and symptoms of...
A Case of Immature Intrapericardial Teratoma
Hea Young Shin, Won Kju Choe, Hae Yong Lee, Chong Kook Lee, Keun Chang Song, Soon Hee Jung
Clin Exp Pediatr. 1994;37(1):129-134.   Published online January 15, 1994
This paper describles a case of intrapericardial teratoma in a 20-day-old female neonate, who suffered from cyanosis and respiratory difficulty. She was evaluated by echocardiography, chest CT and MRI, the suspected intrapericardial mass was identified and surgically removed. The postoperative diagnosis was intrapericardial teratoma, grade II. This case is reported with brief review of some related literature.
A Case of Sacrococcygeal Teratoma with Spina Bifida Cystica in Newborn
Tae Woo Kim, Sung Ki Park, Young Soo Baik, Hee Sin Ko, Dong Uk Kim, Woo Taek Kim, Woong Hm Kim, Chang Yeun Lee, Young Bae Lee
Clin Exp Pediatr. 1993;36(12):1747-1751.   Published online December 15, 1993
Sacrococcygeal teratoma is a rare tumor, it occurs once in every 40,000 live births. Most of the reported cases appear in female infant (M:F=1:4). They deserve clinical attention because they are potenially malignant and are curable if diagnosed and treated early. The patients may have associated congenital anomalies. This patient has spina bifida cystica in lower sacrum. Brief review of related literature is included...
Original Article
A case of gastric teratoma.
Young Sup Shin, Hwa Ja Kim, Sang Kyu Park, Ho Jin Park, Chang Hyun Lee, Joung Ha Son, Mi Kyung Shin
Clin Exp Pediatr. 1991;34(9):1311-1315.   Published online September 30, 1991
Gastric teratoma is a benign tumor that occurs rarely, is found most frequently in male infants, and is best treated by excision. A 3-month-old male patient had abdomial mass and dyspnea due to gastinc teratoma. The literature on this subject was reviewed briefly.
A Case of Sacrococcygeal teratoma complicated by hydronephrosis and hydroureter.
Joo Saeng Moon, Sung Ki Jin, Doo Sung Moon, Kyung Sook Cho, Jong Dae Cho, In Ki Sung, Bo Hyun Han
Clin Exp Pediatr. 1988;31(1):134-140.   Published online January 31, 1988
The authors experienced a case of benign cystic sacrococcygeal teratoma in a 2 month-old female infant. The cystic mass was located at presacral area without external presentation, causing left renal hydronephrosis and ureterectasis. Surgical excision of the mass was performed successfully. The literature regarding the subject was reviewed.
Case Report
A Cases of Retroperitoneal Immature Teratoma(Grade III).
A Ellen Kim, Hee Ju Kim, Jae Sun Jung, Sung Ill Ahn, Hye Kyung Lee, Je Geun Chi
Clin Exp Pediatr. 1987;30(3):327-334.   Published online March 31, 1987
Je Geun Chi, M.D. Department of Pathology, College of Medicine, Seoul National University, Seoul, Korea We herein presented a case of retroperitoneal immature teratoma in a 4 month-old boy who had a huge intra abdominal mass with hypertension, sweating and loose stool. The pre-op diagnosis as well as a post-op diagnosis was a intrarenal mass (R/0 Wilms' tumor) which was later confirmed to be a...
A case of Sacrococcygeal Teratoma.
Seung Jae Yang, Kwang Nam Kim, In Joon Seol, Soo Jee Moon, Keun Soo Lee
Clin Exp Pediatr. 1986;29(5):564-569.   Published online May 31, 1986
We exprienced a case of sacrococcygeal teratoma in newborn girl with massive intraabdominalfextensioii and small caudal mass, which is relative rare.
Original Article
Two Cases of Teratoma on Sacrococcygeal Region in Newborn.
Chan Uhng Joo, Young Suk Jang, Jung Soo Kim, Kyu Cha Kim
Clin Exp Pediatr. 1982;25(8):859-863.   Published online August 31, 1982
Two cases of teratoma on sacrococcygeal region in newborn are reported with pathological findings, and a brief review of related literature is included in this report.
Case Report
A Case of Gastric Teratoma Combined with Congenital Syphilis.
Du Yung Lee, Jin Sook Lee, Dong Whan Cha, Se Jin Kang, Kwang Ho Kim, Kwan Sub Chung
Clin Exp Pediatr. 1982;25(4):404-409.   Published online April 30, 1982
Gastric Teratomas are exetremely rare in infancy and childhood. About 50 cases of gastric teratomas are reported in the world's literature. Most of them were male. Few were dignosed prior to surgery. The mos thelpful diagnostic aid was of teeth or bone in radiologic examinations. Treatment is surgical excision and all of them were benign. Recently, we experienced a case...
A Case of Mediastinal Teratoma in Early Childhood.
Kil Su Kim, Youn Mo Shon, Myung Hi Shin, Ji Sub Oh
Clin Exp Pediatr. 1982;25(3):305-309.   Published online March 31, 1982
We experienced a case of anterior mediastinal teratoma in 26 month old boy with 2 month history of cough and dyspnea. The diagnosis was easily established by chest CAT which revealed calcific densities, while plane radiographs of chest revealed no evidence of calcification. Operation was done with good result and remained in good condition thereafter. A brief of the related...