Abstract
Histiocytosis syndrome is not rare disease of unknown etiology, characterized by development of granulomatous lesions with histiocytic proliferation. Authors analyzed 22 cases, which had been confirmed as histiocytosis syndrome from 1971 to Feb. 1980 with special attention to 15 cases showing positive findings on radiological examinations. The results are as follows. 1. Overall male to female ratio was about 2:1. The majority were between 1 and 7 years of age. 2. Skeletal system was involved in orders as follows: skull, pelvis, femur, rib, spine. 3. Four cases of pulmonary involvement were experienced. All cases had interstitial involvement with reticulonodular densities on roentgenograms. 4. We had experienced a pituitary tumor, presumably localized histiocytic mass, in a patient with diabetes insipidus. 5. In long bone involvement, diaphysis or metaphysis was usually involved, but in one patient, lesion were extended into epiphysis. 6. One case of platyspondyly was found, with symmetrical compression.
Hong, Sung Mo;
Cho, Byung Jae;
Yeon, Kyung Mo
[1]
- College of Medicine, Seoul National University, Seoul (Korea, Republic of)
Citation Formats
Hong, Sung Mo, Cho, Byung Jae, and Yeon, Kyung Mo.
Radiologic features in histiocytosis syndrome.
Korea, Republic of: N. p.,
1980.
Web.
Hong, Sung Mo, Cho, Byung Jae, & Yeon, Kyung Mo.
Radiologic features in histiocytosis syndrome.
Korea, Republic of.
Hong, Sung Mo, Cho, Byung Jae, and Yeon, Kyung Mo.
1980.
"Radiologic features in histiocytosis syndrome."
Korea, Republic of.
@misc{etde_21051549,
title = {Radiologic features in histiocytosis syndrome}
author = {Hong, Sung Mo, Cho, Byung Jae, and Yeon, Kyung Mo}
abstractNote = {Histiocytosis syndrome is not rare disease of unknown etiology, characterized by development of granulomatous lesions with histiocytic proliferation. Authors analyzed 22 cases, which had been confirmed as histiocytosis syndrome from 1971 to Feb. 1980 with special attention to 15 cases showing positive findings on radiological examinations. The results are as follows. 1. Overall male to female ratio was about 2:1. The majority were between 1 and 7 years of age. 2. Skeletal system was involved in orders as follows: skull, pelvis, femur, rib, spine. 3. Four cases of pulmonary involvement were experienced. All cases had interstitial involvement with reticulonodular densities on roentgenograms. 4. We had experienced a pituitary tumor, presumably localized histiocytic mass, in a patient with diabetes insipidus. 5. In long bone involvement, diaphysis or metaphysis was usually involved, but in one patient, lesion were extended into epiphysis. 6. One case of platyspondyly was found, with symmetrical compression.}
journal = []
issue = {2}
volume = {16}
place = {Korea, Republic of}
year = {1980}
month = {Dec}
}
title = {Radiologic features in histiocytosis syndrome}
author = {Hong, Sung Mo, Cho, Byung Jae, and Yeon, Kyung Mo}
abstractNote = {Histiocytosis syndrome is not rare disease of unknown etiology, characterized by development of granulomatous lesions with histiocytic proliferation. Authors analyzed 22 cases, which had been confirmed as histiocytosis syndrome from 1971 to Feb. 1980 with special attention to 15 cases showing positive findings on radiological examinations. The results are as follows. 1. Overall male to female ratio was about 2:1. The majority were between 1 and 7 years of age. 2. Skeletal system was involved in orders as follows: skull, pelvis, femur, rib, spine. 3. Four cases of pulmonary involvement were experienced. All cases had interstitial involvement with reticulonodular densities on roentgenograms. 4. We had experienced a pituitary tumor, presumably localized histiocytic mass, in a patient with diabetes insipidus. 5. In long bone involvement, diaphysis or metaphysis was usually involved, but in one patient, lesion were extended into epiphysis. 6. One case of platyspondyly was found, with symmetrical compression.}
journal = []
issue = {2}
volume = {16}
place = {Korea, Republic of}
year = {1980}
month = {Dec}
}