1.Signet Ring Cell Variant of Invasive Lobular Carcinoma of Male Breast.
Seung Sam PAIK ; Seok Hoon JEON ; Moon Hyang PARK ; Pa Jong JUNG ; Jung Dal LEE
Korean Journal of Pathology 1997;31(2):179-181
Lobular carcinoma of the male breast is very rare, because of the absence of lobules in the normal male breast. Herein, a case of lobular carcinoma of the male breast with cellular features of signet ring cells is described. A 57-year-old man presented with a left breast mass. Histologic examination showed classic invasive lobular carcinoma with in situ component. Most infiltrating tumor cells had a prominent signet ring cell appearance. The patient was phenotypically male and had fathered children. There was no history of predisposing factors to breast lesion, such as hormone use or gynecomastia.
Breast*
;
Carcinoma, Lobular*
;
Causality
;
Child
;
Fathers
;
Gynecomastia
;
Humans
;
Male*
;
Middle Aged
2.Signet Ring Cell Variant of Invasive Lobular Carcinoma of Male Breast.
Seung Sam PAIK ; Seok Hoon JEON ; Moon Hyang PARK ; Pa Jong JUNG ; Jung Dal LEE
Korean Journal of Pathology 1997;31(2):179-181
Lobular carcinoma of the male breast is very rare, because of the absence of lobules in the normal male breast. Herein, a case of lobular carcinoma of the male breast with cellular features of signet ring cells is described. A 57-year-old man presented with a left breast mass. Histologic examination showed classic invasive lobular carcinoma with in situ component. Most infiltrating tumor cells had a prominent signet ring cell appearance. The patient was phenotypically male and had fathered children. There was no history of predisposing factors to breast lesion, such as hormone use or gynecomastia.
Breast*
;
Carcinoma, Lobular*
;
Causality
;
Child
;
Fathers
;
Gynecomastia
;
Humans
;
Male*
;
Middle Aged
3.A Case of Hereditary Anhidrotic Ectodermal Dysplasia.
Jong Won LEE ; Jin Kyung JUNG ; Jin Gun BANG ; Jin Sam RHO ; Jung Hee PARK
Journal of the Korean Pediatric Society 1994;37(10):1453-1456
Hereditary anhidrotic ectodermal dysplasia is a rare condition characterized by underdeveloped ectodermal structure including the skin, teeth or skin appendages. The patient has characteristic feature of anhidrosis, hypotrichosis and defective dentition. We experienced a case of hereditary anhidrotic ectodermal dysplasia in a l-month-old male infant who had unexplained recurring fever, anhidrosis and characteristic facial feature, so we established the diagnosis with clinical feature and skin biopsy.
Biopsy
;
Dentition
;
Diagnosis
;
Ectoderm
;
Ectodermal Dysplasia*
;
Fever
;
Humans
;
Hypohidrosis
;
Hypotrichosis
;
Infant
;
Male
;
Skin
;
Tooth
4.Ureteral Fibroepithelial Polyp: A report of four cases (One case with nephrogenic adenoma).
Won Mee LEE ; Seung Sam PAIK ; Eun Kyung HONG ; Moon Hyang PARK ; Jung Dal LEE
Korean Journal of Pathology 1996;30(8):715-720
Fibroepithelial polyps of the ureter are usually acquired rather than congenital. Most polyps are hamartomatous growths which tend to arise in the proximal portion of the left ureter. Most patients exibit either hematuria or persistent flank pain secondary to partial ureteral obstruction. Because of false positivity of urine cytology, as well as intravenous pyelogram, the correct diagnosis is confused with malignancy. Herein we report four cases of ureteral fibroepithelial polyp, which are associated with stones resulting in partial obstruction of the ureter. One of the four cases is associated with nephrogenic adenoma in the lamina propria of the adjacent ureter. The following report describes clinicopathologic findings of fibroepithelial polyp with review of literatures.
Adenoma
5.Histological Study of Ductus Arteriosus Affected by Indomethacin in the Fetal Rates.
Young Sook JANG ; Chang Yeoul JEON ; Heon Sook LEE ; Jung Soo KIM ; Moo Sam LEE
Journal of the Korean Pediatric Society 1983;26(8):770-777
No abstract available.
Ductus Arteriosus*
;
Indomethacin*
6.Congenital Mesoblastic Nephroma.
Seok Hoon JEON ; Seung Sam PAIK ; Nam Hoon KIM ; Moon Hyang PARK ; Jung Dal LEE
Korean Journal of Pathology 1997;31(4):375-378
Mesoblastic nephroma is an important differential diagnosis of a renal mass occurring in the neonatal period or in early childhood. It is a rare monomorphous congenital renal neoplasm most commonly recognized during the first 3 months of life. With the widespread application of ultrasound imaging, many cases are recognized prior to birth. We report a case of mesoblastic nephroma detected by ultrasonograph at 36 weeks of intrauterine fetal life and removed after birth. It showed a well circumscribed, grayish white, solid mass measuring 4x3x2 cm. The tumor was predominantly a classic type with a focal cellular pattern. Immunohistochemical and electron microscopic studies were done.
Diagnosis, Differential
;
Kidney
;
Kidney Neoplasms
;
Nephroma, Mesoblastic*
;
Parturition
;
Ultrasonography
7.In vitro antibacterial potency of teicoplanin by the disc diffusion method.
Pyung Han HWANG ; Jung Soo KIM ; Yang Keun LEE ; Mi Ae YOON ; Sam Im CHOI
Korean Journal of Infectious Diseases 1993;25(1):33-43
No abstract available.
Diffusion*
;
Teicoplanin*
8.Idiopathic Entero-colic Lymphocytic Phlebitis: A case report.
Seung Sam PAIK ; Young Ha OH ; Eun Kyung HONG ; Jung Dal LEE
Korean Journal of Pathology 1996;30(6):533-538
Localized enterocolic lymphocytic phlebitis is characterized by selective phlebitis involving the small to medium-sized veins and venules, infiltration exclusively by lymphocytes, and no other systemic vasculitis or inflammatory bowel disease. This vasculitis can be a rare cause of intestinal ischemia. We experienced a case of enterocolic lymphocytic phlebitis in a 72-year-old woman, who presented with abdominal pain and distension. The resected colon and terminal ileum showed striking lymphocytic phlebitis affecting the veins and venules of the bowel and mesentery which resulted in ischemic injury of the bowel. This vasculopathy was the only demonstrable cause of ischemia. Arteritis and arteriolitis was not found. There is no clinical or laboratory evidence or a history of extraintestinal vasculitis. The etiology of this clinicopathological entity has not been elucidated. Herein, we report the clinicopathological findings in this patient who presented with ischemic intestinal necrosis caused by localized intestinal lymphocytic phlebitis associated with thrombosis.
Female
;
Humans
9.Inflammatory Myofibroblastic Tumor in Posterior Mediastinum.
Seung Sam PAIK ; Seok Hoon JEON ; Se Jin JANG ; Moon Hyang PARK ; Jung Dal LEE
Korean Journal of Pathology 1997;31(1):63-67
Inflammatory myofibroblastic tumor(IMT) or inflammatory pseudotumor is a rare, solid tumor that most often affects children. This tumor is characterized by a spindle cell proliferation admixed with a variety of inflammatory cells. Although it has disputed nosology, a distinctive fibroinflammatory and even pseudosarcomatous appearance have been well appreciated. Herein, we report a case of IMT in the posterior mediastinum in a 19-year-old girl with clinical findings. The immunohistochemical and ultrastructural studies on the tumor cells are reported, and their distinctive characteristics are discussed in details.
Cell Proliferation
;
Child
;
Female
;
Granuloma, Plasma Cell
;
Humans
;
Mediastinum*
;
Myofibroblasts*
;
Young Adult
10.The Change of Causes of Upper Gastrointestinal Bleeding.
Hyun Jung KIM ; Sam Beom LEE ; Byung Soo DO ; Tae Nyeun KIM ; Moon Kwan CHUNG
Journal of the Korean Society of Emergency Medicine 1999;10(2):227-241
Upper gastrointestinal(UGI) bleeding was critical disease that was commonly found in emergency department and needed more early diagnosis and rapid treatment for decreasing mortality and morbidity. It's causes and frequencies here affected by many factors, but the majorities were caused by peptic ulcers and esophageal-gastric varices. With development of economy and medical services, new drugs and endoscopic interventions, the treatment of patients with UGI bleeding was more improved. So I would like to evaluate the change of causes and frequencies of UGI bleeding and the associated clinical findings. A total of 1,546 patients presented with UGI bleeding in emergency department of Yeungnam university hospital during the five years from Jan. 1991 to Dec. 1995 were clinically reviewed by charts and compared with previous seven years report from Jan. 1984 to Dec. 1990 in the same hospital. The ratio of male to female was 6.1:1 and slightly increased in comparison with previous seven years. The incidences in 6th and 5th decades were highest(54.4%) as like as previous seven years. Age distribution of duodenal ulcer bleeding, Mallory-Weiss tear and acute gastric mucosal lesion were developed in lower decades than the others. The causes of UGI bleeding were caused by esophageal varix(45.4%), peptic ulcer(38.8%), Mallory-Weiss tear(4.3%), gastric cancer(3.8%), others(3.1%), acute gastric mucosal lesion(2.7%), undetermined causes(1.8%) in defending order of frequencies. The proportion of esophageal varices was increased from 36.6% to 45.4%, but that of peptic ulcer was relatively decreased from 47.6% to 38.8%. And the annual distribution of varices was increased, however the annual distribution of peptic ulcers was increased. Although the ranking of annual distribution of gastric ulcers and duodenal ulcers were not changed compared to previous study and the frequency of gastric ulcers was increased since 1992, but additional follow-up was needed. Seasonal variations were found that upper gastrointestinal bleeding was increased in fall and peptic ulcer bleeding was increased significantly in summer and fall, however, varix bleeding was less frequent in summer time as like as previous seven years. Emergency endoscopic examination was performed within 6 hours far 54.5%, 24 hours for 90.8% and this reacts were to be like previous results, 57.5% and 90.7% respectively. Findings of emergency endoscopic examination were active bleeding focus(21.2%), blood clot(7.9%), exposed vessels(13.3%), flat blood spot(6.4%) and lesion without evidence of bleeding(51.3%). Endoscopic findings of active bleeding were easily seton when examination was perfomed within 24 hours. Blood transfusion was performed in 67.3% with average 2.1 units. When the causes of bleeding were due to varix and marginal ulcer, more amounts of blood were transfused than the others. In previous seven years, blood transfusions were performed in 71.2% with average 5 units and more amounts of blood were transfused in gastric cancer and varix bleeding.
Age Distribution
;
Blood Transfusion
;
Duodenal Ulcer
;
Early Diagnosis
;
Emergencies
;
Emergency Service, Hospital
;
Esophageal and Gastric Varices
;
Female
;
Follow-Up Studies
;
Hemorrhage*
;
Humans
;
Incidence
;
Male
;
Mallory-Weiss Syndrome
;
Mortality
;
Peptic Ulcer
;
Seasons
;
Stomach Neoplasms
;
Stomach Ulcer
;
Varicose Veins