1.Basaloid-Squamous Carcinoma of the Esophagus: A case report.
Korean Journal of Pathology 1992;26(1):96-98
Basaloid-squamous carcinoma of the esophagus is rare and similiar to the solid type of adenoid cystic carcinoma of the salivary gland. The origin of this tumor is unknown. The tumor was located in the lower third of the esophagus. The case of basaloid-squamous carcinoma consisted of submucosal tumor showing carcinoma with a basaloid pattern and focal squamous differentiation associated with squamous cell carcinoma or carcinoma in situ of the esophageal mucosa. A few submucosal tumor cells were positive for cytokeratin.
2.Congenital Cystic Adenomatoid Malformation of the Lung: A report of 3 cases.
Kyi Beom LEE ; Woo Hee JUNG ; In Joon CHOI
Korean Journal of Pathology 1985;19(4):431-437
Congenital cystic adenomatoid malformation of the lung is a rare form of congenital cystic disease of the lung and associated with developmental arrest of bronchioles in embryonic life. We report 3 cases of congenital cystic adenomatoid malformation which are classified as type I, II and III according to the morphological classification by Stocker et al. The first case was a 6-year-old female with a mass in the lower lobe of the right lung. The mass was composed of several cysts which were filled with inflammatory exudate and lined by ciliated pseudostratified columnar epithelium (type I + II). The second case was a 4-year-old female with a mass in the middle lobe of the right lung. It was composed of numerous small cysts which were uniform sized and contained inflammatory exudate. These were lined by ciliated columnar and pseudostratified columnar epithelium (type II). The third case was a stillborn female at 27 weeks of gestation. There was generalized edema and severe ascites. The left lower lobe consisted of an ill-defined solid area and small cysts. The solid lesion was composed of bronchiole-sized cysts lined by non-ciliated cuboidal epithelium (type II + III).
Female
;
Humans
;
Cysts
3.Five cases of abdominal sacral colpopexy for the vaginal vault prolapse after total hysterectomy.
Sang Joon CHOI ; Kyung LEE ; Young Gyul KIM ; Hyuk JUNG
Korean Journal of Obstetrics and Gynecology 1999;42(10):2377-2381
A rate com;lication of hysterectomy is complete prolapse and inversion of vagina. This can occur whether the hysterectomy was abdominal or vaginal and cystocele and/or enterocele is often associated with this condition. Traditionally, prolapse has been treated by surgery, the types of operation for prolapse are generally but not always, carried out through the vaginal rather than through the abdominal surgical route. We experienced five cases who had repair of posthysterectomy vaginal vault prolapse by transabdominal sacral colpopexy and report with brief review of literatures.
Cystocele
;
Hernia
;
Hysterectomy*
;
Pelvic Organ Prolapse*
;
Prolapse
;
Vagina
4.Clear Cell Sarcoma of Tendons and Aponeuroses: A case report with electron microscopic examination.
Woo Hee JUNG ; Kyu Rae KIM ; In Joon CHOI
Korean Journal of Pathology 1985;19(2):244-249
Clear cell sarcoma of tendons and aponeuroses is the term coined by Enzinger in 1965 to describe a rare but unique type of soft tisse neoplasm whose cells characteristically have the capacity to produce melanin. The authors experienced a case of 64-year old female who presented with a 6x5x4 cm sized mass deeply seated in the left popliteal fossa. The mass was firm and multinodular, and on cut section revealed patches of brown black pigmentation. Histologically the tumor was composed of round to fusiform cells with clear or pale eosinophilic cytoplasm that contained small amounts of glycogen, separated into compact nests or short fascicles by delicate septa of fibrous tissue. The brown black pigment seen in tumor cells and stroma was proven to be melanin by special stain, and ultrastructural examination showed melanosomes in varying stages of development dispersed freely in the cytoplasm or in the lysosomes. These findings strongly support the view that clear cell sarcoma is a tumor of neural crest origin rather than of tenosynovial mesenchyme origin, and is a soft tissue variant of malignant melanoma.
Female
;
Humans
5.Various appearances of rib companion shadow mimicking a pathologic condition.
Ye Won CHOI ; Shi Joon YOO ; Jung Gi IM
Journal of the Korean Radiological Society 1992;28(1):78-83
We have observed that the companion shadow of the upper rib may be misinterpreted as a small pnemothorax or pleural plaque associated with asbestosis. To observe the radiographic characteristics of the normal companion shadow, we analyzed, on the posteroanterior(PA) chest radiographs, the companion shadow of 50 normal cases. Factors such as occurrence on each rib, the sharpness of the margin, the relative position to the rib, the shape and the thickness were observed. Also, we analyzed the displaced pleura of 4 pneumothorax cases to differentiate their frndings from the findings of normal companion shadows. On 50 normal chest radiographs, 192 compaion shadows were observed on the first to fourth ribs. In 173 of those shadows, the visceral margin of the companion shadow on the second rib simulated pneumothorax more closely than those on any othe rivs due to its apical location and thinness. In six of 50 normal cases, the companion shadow on the first or second rib showed an inw rdly convex lower margin, mimicking pleural plaque. The compaion shadow was suggested on the plain chest radiograph by the following characteristics imultiplicity(47/50), thicker than normal pleura(3/4), persistent on serial filma with the same shape and specific location(4/4).
Asbestosis
;
Friends*
;
Humans
;
Pleura
;
Pneumothorax
;
Radiography, Thoracic
;
Ribs*
;
Thinness
6.Correction of deviated nose using reverse swinging door precedure.
Joon Yong CHOI ; Jae Seung LEE ; Jae Jung KIM ; Bom Joon HA ; Myoung Soo SHIN
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1999;26(6):1107-1111
There have been so many methods described for the correction of the deviated noses but it is difficult to get satisfactory results and recurrence rate is high. There is no exact explanation why the recurrences are so high and no estabished guides for techniques according to the surgical pathology. We found the classical swinging door technique effective in cases where the caudal septum deviated from the midline. However, where the caudal septum and the tip stay in the midline, scoring or submucosal resection do not work well enough to cortet them. We used the reverse swinging door technique of our own. After elevation of mucoperichonodrium, we did sagittal section in the posterior septum and moved the septum to the midline on the pivot point of the caudal septum and. The gap created in the posterior portion of the septum were filed with bone grafts, cartilage grafts or Medopor, which were sutured to the septum, We did this technique with or without osteotmies in 56 deviated noses for last 5 years. The results were very satisfactory and there was no complication.
Cartilage
;
Nose*
;
Pathology, Surgical
;
Recurrence
;
Transplants
7.A Case of Congenital Nephrotic Syndrome.
Choong Sun KANG ; Chang Hee HWANG ; PyungKil KIM ; Hyeon Joo JEONG ; In Joon CHOI ; Jung Hye CHOI
Journal of the Korean Pediatric Society 1988;31(5):627-634
No abstract available.
Nephrotic Syndrome*
8.A Case of Reye Syndrome Following Treatment of Kawasaki Disease with Aspirin.
Joon Kee LEE ; Ji Eun KANG ; Eun Hwa CHOI ; Jung Yun CHOI
Korean Journal of Pediatric Infectious Diseases 2012;19(2):79-83
Reye syndrome is a rapidly progressive encephalopathy with hepatic dysfunction, which often begins several days after apparent recovery from a viral illness, especially varicella or influenza A or B. Salicylate use was identified as a major precipitating factor for the development of Reye syndrome. With the recommendation to avoid use of salicylates in children, Reye syndrome has virtually disappeared in recent years. We report a case of Reye syndrome in a 5-month-old infant who had been treated with intravenous immunoglobulin and aspirin under the diagnosis of Kawasaki disease, and showed symptoms of sudden onset of irritability, rigidity, decreased activity, vomiting, poor appetite, lethargy, liver dysfunction without jaundice, coagulopathy, and hyperammonemia.
Appetite
;
Aspirin
;
Chickenpox
;
Child
;
Humans
;
Hyperammonemia
;
Immunoglobulins
;
Infant
;
Influenza, Human
;
Jaundice
;
Lethargy
;
Liver Diseases
;
Mucocutaneous Lymph Node Syndrome
;
Precipitating Factors
;
Reye Syndrome
;
Salicylates
;
Vomiting
9.Histopathological and Immunohistochemical Studies of Primary Gastrointestinal Lymphomas in Korean Patients.
Soon Hee JUNG ; Hyen Joo JEONG ; Woo Hee JUNG ; Tai Seung KIM ; In Joon CHOI
Korean Journal of Pathology 1987;21(3):153-167
The present study is aimed to investigate the clinical and pathologic features of GI lymphomas and the immunocytochemical characteristics, using 71 cases of primary GI lymphomas examined at the Department of Pathology, Yonsei University College of Medicine, Youngdong Serverance Hospital and Yonsei University Wonju College of Medicine from January, 1976 to December, 1985. Results obtained were as follows: 1) Sixty eight cases were Non-Hodgkin's lymphoma and 3 Hodgkin's lymphoma. Surgical resection was done in 58 patients and surgical biopsy in 13. 2) The primary sites of the tumors were stomach, small intestine, ileocecal area and large intestine in a descending order of frequency. 3) The mean age at the time of diagnosis was 45 years. The tumor of the small intestine was generally detected in the younger age and that of the large intestine in the older age. The overall male to female ratio was 1.9 : 1. 4) Abdominal pain was the most common presenting symptom irrespective of the sites of the tumor. Duration of the symptoms were evenly distributed from hours to 12 monthes. 5) The size of the tumors was less than 10 cm in the largest dimension in most of the cases (79.3%). The gross types of the GI lymphomas were ulcerative (27.6%), polypoid (20.7%), multinodulated (17.2%) and diffuse thickening. The rate of lymph node involvement was 44.4% in tumors confined to the serosa, while 82.6% in tumors with serosal penetrations. 6) Classification of 68 cases of Non-Hodgkin's lymphoma according to Working Formulation revealed 50 cases of intermediate grade, 13 cases of high grade and 5 cases of low grade. According to Rappaport classification, all were diffuse types, among which diffuse histiocytic type was the most common. According to Lukes-Collins classification, 60 cases were B cell types, 4 cases genuine histiocytes types and 3 cases T cell types. Most of the gastric and intestinal lymphomas belonged to the follicular center cell (small and large cleaved, large cleaved) types. 7) Immunoperoxidase stains were done in 55 cases of malignant lymphomas. Thirty (65.9%) of 47 B cell lymphomas revealed a positivity for B cell markers. Twenty three (48.9%) of them showed a monoclonality, in which kappa/IgG pattern was most frequently demonstrated. Four cases of true histiocytic lymphomas were positive for alpha-1-antichymotrypsin and lysozyme, the former of which was seemed to be a more sensitive marker for histiocytic differentiation. An attempt was made to evaluate the significance of the degree of reactive histiocytic infiltrates within the lymphoma in relation to the progosis, but correlation could not be made because of the limited cases.
Female
;
Male
;
Humans
;
Biopsy
10.A Clinical Study on the Ovarian Tumors in Pregnancy.
Yong Gul KIM ; Tae Jung KIM ; Hyun Jung LIM ; Sang Joon CHOI ; Chang Hun SONG ; Sei Jun HAN ; Hyuk JUNG
Korean Journal of Perinatology 2001;12(1):35-43
No abstract available.
Pregnancy*