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Case Report
Melanotic Neuroectodermal Tumor of Infancy in the Epididymis : A Case Report
Sang Bae Lee, Seong Hun Lee, Min Hyuk Ryu, Ji Seoung Park, Joo Heoun Yang, Sun Young Kim, Dong Jean Lee
Clin Exp Pediatr. 2004;47(12):1334-1337.   Published online December 15, 2004
Melanotic neuroectodermal tumor of infancy (MNTI) is a rare neoplasm known by a variety of names including melanotic progonoma and retinal anlage tumor, and currently thought to be neural crest derivation. The vast majority develop within the first year of life. The behavior is generally benign, but recurrent and metastatic cases have been documented. It arises in the head and...
A Case of Primitive Neuroectodermal Tumor of the Adrenal Gland
Sun Pil Jung, Chong Gwon Oh, In Seok Lim, Dong Keun Lee, Byoung Hoon Yoo
Clin Exp Pediatr. 2001;44(12):1459-1462.   Published online December 15, 2001
Primitive neuroectodermal tumors(PNETs) are a group of small round cell tumors that may arise in the central or peripheral nervous system. In the extracranial location, these neoplasms may occur anywhere and at any age group, but most likely in the bone and soft tissue of children and young adults. The incidence of adrenal gland involvement is very rare. This tumor...
Herditary Anhidrotic Ectodermal Dysplasiain Twins
Myung Gil Han, Do Hyun Kim, Hyung Ro Moon
Clin Exp Pediatr. 1996;39(7):1005-1009.   Published online July 15, 1996
Hereditary anhidrotic ectodermal Dysplasia is a congenital disease displaying characteristics of anhidrosis, hypotrichosis and dental defect which are caused by developmental anomaly of ectodermal epidermis and its appendages. We experienced two cases of hereditary anhidrotic ectodermal dysplasia in two-year and four-month old twin brothers. These patients suffered from intermittent high fever early in life which brought them to our clinical attention. However the diagnosis of...
A Case of Hereditary Anhidrotic Ectodermal Dysplasia
Jong Won Lee, Jin Kyung Jung, Jin Gun Bang, Jing Sam Rho, Jung Hee Park
Clin Exp Pediatr. 1994;37(10):1453-1456.   Published online October 15, 1994
Hereditary anhidrotic ectodermal dysplasia is a rare condition characterized by underdeveloped ectodermal structure including the skin, teeth or skin appendages. The patient has characteristic featureof anhidrosis, hypotrichosis and defective dentition. We experienced a case of hereditary anhidrotic ectodermal dysplasia in a 1-month-old male infant who had unexplained recurring fever, anhidrosis and characteristic facial feature, so we established the diagnosis with clinical...
Original Article
A Case of Hypohydrotic Ectodermal Dysplasia.
Chun Oh Lee, Byung Min Moon, Young Wook Kim, Ki Bok Kim
Clin Exp Pediatr. 1990;33(12):1718-1722.   Published online December 31, 1990
Hypohidrotic ectodermal dysplasia is a group of disorders characterized characterized by faulty development of ectodermal structures including the skin, teeth, skin appendages, resulting in hypohi- drosis, hypotrichosis, and abnormal dentition. Here, we report a case of typical hypohidrotic ectodermal dysplasia in a 16-month-old male who had unexplained recurring fever, hypohidrosis, hypotrichosis, anodontia, and characteristic facial features.
Case Report
A Cases of Heredotary Anhidrotic Ectodermal Dyslasia.
Jong Soo Kim, Pyoung Han Hwang, Hyeon Sook Lee, Jung Soo Kim
Clin Exp Pediatr. 1983;26(10):1018-1023.   Published online October 31, 1983
Hereditary anhidrotic ectodermal dysplasia is a rare hereditary condition in which certain structures derived from the ectoderm are undeveloped or underdeveloped, although, on a rarity, mesodermal or endodermal derivatives may be associated. Recently, we have experienced a case of anhidrotic ectodermal dysplasia in 4 years old male. He had abscence of sweating, hypotrichosis and anodontia, which was characteristic features of this disorder. We established...
There cases of Hereditary Anhidrotic Ectodermal Dysplasia.
Seung Woo Moon, Seung Koo Park, Jung Ju Kim, Dong Hak Shin, Sang Suk Lee
Clin Exp Pediatr. 1982;25(1):80-88.   Published online January 31, 1982
Hereditary anhidrotic ectodermal dysplasia is a rare hereditary condition in which certain structures derived from the ectoderm are undeveloped or underdeveloped, although, on a rarity, mesodermal or endodermal derivatives may be associated. Recently, we enperienced 3-cases of anhidrotic ectodermal dysplasia in 3 months male infant and in brothers aged 4(1/2) months and 22 months. They had abscence of sweating, hypotrichosis...