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Case Report
A Case of Agenesis of the Right Lung
Hyun Soon Lee, Gyeong Cheol Yoon, Se Wook Oh, Ho Seek Ahn, Sung Won Kim, Chung Hee Chi
Clin Exp Pediatr. 1992;35(2):240-244.   Published online February 15, 1992
Unilateral lung agenesis is defined with absence of parenchyme, supporting structures and airway below the level of the carina. Lung agenesis is associated with other anomaly of cardiovascular system, musculoskeletal system and genitourinary system in about 50% cases. In most cases, the diseases is found due to respiratoru problems. Prognosis is variable but largely depends on the associated anomaly and...
A Case of Epidermolysis Bullosa Dystrophica.
Soon Yol Hwang, Jeong Sil Han, Gu Seok Jung, Sung Won Kim, Kil Hyun Kim, Chung Hee Chi
Clin Exp Pediatr. 1987;30(9):1049-1054.   Published online September 30, 1987
Epidermolysis bullosa dystrophica (EBD) is a rare, chronic noninflammatory mechanobullous disease of hereditary trait, which easily produces bulla by minor injury or spontaneously. We experienced a case of EBD in a 27th day of life female patient. Diagnosis was confirmed by clinical features, light and electron microscopy. A brief review of related literature was made.
A Case of Letterer-Siwe Disease.
Suh Hong Ha, Jeong Sil Han, Sung Won Kim, Kyung Tae Kim, Kil Hyun Kim, Chung Hee Chi
Clin Exp Pediatr. 1987;30(3):335-341.   Published online March 31, 1987
Letterer-Siwe disease is a variant of Histiocytosis X and characterized by onset in infancy, hepatosplenomegaly, lymphadenopathy, bleeding tendency, hypochromic anemia, fever, localized bone defect and fatal outcome. The diagnosis was confirmed by clinical symptoms, laboratory datas, histopathologic and radiologic findings. We experienced a case which was treated by single prednisolone method and resulted to good response. A brief review of literature was made.
Two cases of Retroperitoneal Teratoma
Jwa Sin Kim, Tae Kyu Park, Keun Chan Sohn, Keun Soo Lee, Chung Hee Chi
Clin Exp Pediatr. 1969;12(6):335-340.   Published online June 30, 1969
Two cases of Retroperitoneal Teratoma in two and half months old infants were reported. The diagnosis was established by the clinical, pathological and X-ray findings and surgical removal. The treatment was performed by successful removal, results were excellent. Review o£ Literatures as for Retroperitoneal Teratoma was made briefly.