1.Clinical Review of Miliary Tuberculosis.
Kwangtae CHUNG ; Jingon JUN ; Jahoon KOO
Journal of the Korean Pediatric Society 1979;22(5):360-365
A clinical study was made on 26 children with miliary tuberculosis, who were admitted to the Pediatric department of Kyungpook national university hospital during the period of July, 1973 through June, 1978. Following results were obtained: There was no significant annual difference. However, the highest incidence was noted in the spring(46.2%). Children under the age of 6 were affected most frequently (76.9%), especially under the age of 1(30.8%). Contact history to a known tuberculous patients was noted in 23%(either parents or relatives), and BCG vaccination in younger age was given only in 23.1%. The chief complaints on admission, in order of frequency, were as follows: fever(42.3%), general weakness, dyspnea, coughing, headache, etc. And abnormalities on physical findings were hepatomegaly(53.8%), followed by auscultatory abnormality of the lung(42.3%), neurologic abnormality(42.3%), etc. Tiberculin test using 1 unit of PPD was positive in 36.4%. Hematologic abnormalities were as follow: ESR over 20mm/hr. in 44.4%, hemoglobin less than 11gm% in 53.8%, and increased leucocyte counts on peripheral blood over 10,000/cmm in 50%. AFB culture was positive in 17.6%. Among complications and associated diseases, tuberculous meningitis was the most common one, comprising 42.3%, and sucutaneous emphysema was seen in 2 cases. The mortality rate was 15.4%, 30.8%, in whom follow-up study was possible, showed in all of them improvement after triple therapy, and in most of them, miliary density on the chest x-ray disappeared within 4 months after initiation of antituberculous therapy.
Child
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Cough
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Dyspnea
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Emphysema
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Follow-Up Studies
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Gyeongsangbuk-do
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Headache
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Humans
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Incidence
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Mortality
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Mycobacterium bovis
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Parents
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Thorax
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Tuberculosis, Meningeal
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Tuberculosis, Miliary*
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Vaccination
2.A Case Report of Systemic Mastocytosis.
Kwang Tae CHUNG ; Jahoon KOO ; Sae Kwang MOON
Journal of the Korean Pediatric Society 1979;22(7):546-549
A case of systemic mastocytosis in a 6 year old boy was presented. Skin lesions started to appear and spred several days after birth along with severe itching sensation, and intermitent abdominal pain & constipation developed at the age of 5. On physical examination, he was found to be underdeveloped (Height less than 3rd percentile) with normal vital signs. Liver was felt 1 1/2 fb below costal margin, spleen 2 fb. There were many brown to dark brown-colored irregular shaped maculopapulourticarial skin lesions, scattered all over the body, along with multiple thickened areas, and positive Darier's sign was noted. On upper GI series, many honey-combed filling defect were found throughout small intestine. Skin biopsy confirmed the diagnossis : showing multiple scattered infilteration of mast cells.
Abdominal Pain
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Biopsy
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Child
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Constipation
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Humans
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Intestine, Small
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Liver
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Male
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Mast Cells
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Mastocytosis, Systemic*
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Parturition
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Physical Examination
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Pruritus
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Sensation
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Skin
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Spleen
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Vital Signs