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Original Article
A Case of Pneumocystis Carinii Pneumonia Associated with Cytomegalovirus Lung Infection.
K S Lee, Y O Lee, H J Park, M J Shin
Clin Exp Pediatr. 1987;30(11):1274-1281.   Published online November 30, 1987
Pneumocystis carinii pneumonia has been highly prevalent in prematurity, malnourished infants and immunosuppressed patients. Since 1981, it has been by far the commonest opportunistic infection in AIDS. We experienced a case of Pneumocystis carinii pneumonia associated with cytomegalovirus lung infection in a 3 months old malnourished female orphan. She had been suffered from chronic diarrhea, losing body weight 2 kg in a month prior...
Case Report
Case of Peripheral Neuroepithelioma with Ectopic ACTH Syndrome.
O Y Lee, K S Lee, H I Chung, H J Park, M J Shin, K J Cho, J G Chi
Clin Exp Pediatr. 1987;30(10):1152-1160.   Published online October 31, 1987
Peripheral neuroepithelioma is a rare and controversial neoplasm that may occur at any age. The authors observed the course of a 1-year-old Korean female infant who presented with an enlarging mass in the right hand and manifested hepatic and pulmonary metastases at the time of diagnosis. She also presented with characteristic Cushingoid features, such as moon face, buffalo hump, and truncal obesity. Laboratory...
A Case of Neonatal Varicella.
Y S Chung, K S Lee, H J Park, M J Shin
Clin Exp Pediatr. 1987;30(1):89-93.   Published online January 31, 1987
Three Cases of the Letterer-Siwe Disease.
S H Park, Y C Song, S J Moon, K S Lee
Clin Exp Pediatr. 1980;23(6):501-506.   Published online June 15, 1980
Letterer-Siwe disease is a variant of the three diseases exhibiting similar basic histology and entitled histiocysis X. Eosinophilic granuloma of bone and Hand-Schuller-Christan disease complete the triad. Letterer-Siwe disease is a clinieal-pathologic syndrome characterized by onset in infancy and by generalized hyperplasia of nonlipid-storing macrophages in liver, spleen, Lymph nodes, skin and bone marrow, which usually results in fatal outcome....
A Case of Aeute Werdnig-Hoffmann Disease.
Y M Song, K S Lee, J J Shin, S C Kang, J K Ji
Clin Exp Pediatr. 1978;21(8):623-629.   Published online August 31, 1978
Acute Werdnig-Hoffmann disease is genetically determined progressive degenerative disease of anterior spinal neuron, characterized by fasciculations of the tongue usually occuring along with flaccid paralysis of extremities with intact mentality. We experienced a 5 months old female infant, whose sister died of pneumonia at the age of 2 months, had same symptoms and signs : revealing hypotonic state with flaccid...