1.Epithelioid Leiomyosarcoma of Retroperitoneum: A case report.
Myeng Sun PARK ; Ji Young SEO ; Hae Jin JEONG ; Bang HUR ; Man Ha HUR
Korean Journal of Pathology 1999;33(2):141-144
Epithelioid smooth muscle tumor is relatively rare and potentially malignant, especially in retroperitoneum. Distinct criteria for malignancy still have not been clarified in this epithelioid variant arising in retroperitoneum. We report a deceptively benign-appearing epithelioid leiomyosarcoma in a 50-year-old female. She was admitted with abdominal discomfort and dysuria. Abdominal CT showed a well-demarcated, 10 10 cm sized, solid mass in retroperitoneum. Concomitant metastatic lesions were noted in right lung field. Surgical excision of retroperitoneal mass and right lung lobectomy were performed. The retroperitoneal mass showed yellowish-tan, well-delineated and lobulated appearance. Histologically, this tumor was composed of predominantly epithelioid, round to oval cells with distinct clear cytoplasm and slightly atypical nuclei. Mitosis was rare (0~1/50 HPF). Lung lesions were morphologically similar to that of retroperitoneum.
Cytoplasm
;
Dysuria
;
Female
;
Humans
;
Leiomyosarcoma*
;
Lung
;
Middle Aged
;
Mitosis
;
Smooth Muscle Tumor
;
Tomography, X-Ray Computed
2.Surgical indication and results of patients with CAPD-related peritonitis.
Seong Pil JEONG ; Chul MOON ; Kyung Bal HUR
Journal of the Korean Surgical Society 1992;42(5):662-673
No abstract available.
Humans
;
Peritonitis*
3.Immune response tests by multitest@ CMI and T-cell counts before surgery in the patients with stomach cancer.
Jeong Seon BAEK ; Young Sik SONG ; Kyung Bal HUR
Journal of the Korean Surgical Society 1992;43(2):196-202
No abstract available.
Humans
;
Stomach Neoplasms*
;
Stomach*
;
T-Lymphocytes*
4.Functional & anatomic reconstruction of the donor site after the transverse rectus abdominis myocutaneous(TRAM) flap transfer.
Jeong Seob YOON ; Hur Bum LEE ; Sang Heon LEE ; Keuk Shun SHIN
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1992;19(3):459-469
No abstract available.
Humans
;
Rectus Abdominis*
;
Tissue Donors*
5.Cystic Lymphangioma of the Stomach: A case report.
Soon Ae OK ; Sook Guem JEONG ; Bang HUR ; Man Ha HUH
Korean Journal of Pathology 1993;27(6):670-672
Cystic lymphangiomas of the stomach are extremely rare. These usually present as asymptomatic, polypoid lesion consisting of cystically dilated lymphatic vessels, which are submucosal in location. We report a case of cystic lymphangioma of the stomach. The patient is a 55 year-old woman who has complained of dull pain on epigastrium for 10 years. The mass measures 6x5 cm in cross diameter and is mainly located in the subserosal layer along lesser curvature. Microscopically, the tumor reveals a large number of dilated lymphatic cysts containing serous fluid, lined by a layer of flattened endothelial cells. Ultrastructurally, lining endothelial cells show thin discontinuous basal lamina, in contrast to normal lymphatics.
Female
;
Humans
;
Cysts
6.Balloon Cell Malignant Melanoma: A case report.
Ji Young SEO ; Soon Young KIM ; Jeong Hee KANG ; Young Ok KIM ; Bang HUR
Korean Journal of Pathology 1999;33(7):537-539
Balloon cell malignant melanoma (BCMM) is a rare histologic variant of malignant melanoma, which is composed either predominantly or entirely of large clear or foamy cells. The incidence of balloon cell malignant melanoma is about 0.15% of all cutaneous malignant melanomas. Recently, we experienced a case of cutaneous balloon cell malignant melanoma in the right lower abdomen with right inguinal and both axillary lymph node metastasis in a 56-year-old man. The cutaneous lesion was 4.5 3.5 cm in size, a well-demarcated black nodular mass, involving abdominal skin and subcutaneous tissue. The tumor was histologically composed of two types of tumor cells: predominant clear cell and focal, pigmented spindle cell. The nodal lesion was composed entirely of clear cells. Both clear and spindle cells showed positive reaction for S-100 protein and HMB-45 on immunohistochemistry.
Abdomen
;
Humans
;
Immunohistochemistry
;
Incidence
;
Lymph Nodes
;
Melanoma*
;
Middle Aged
;
Neoplasm Metastasis
;
S100 Proteins
;
Skin
;
Subcutaneous Tissue
7.Claude Syndrome in Midbrain Infraction.
Yang Ki MINN ; Ji Hoe HUR ; Jeong Yeon KIM
Journal of the Korean Neurological Association 1996;14(3):832-835
Claude syndrome is a well known midbrain syndrome which is characterized by ipsilateral oculomotor nerve palsy and contralateral cerebellar ataxia by the lesion of the red nucleus. Although this syndrome was reported as early as in 1924 by Claude, only a few cases have been reported. Moreover, the midbrain infarction as a cause of Claude syndrome has quite rarely been described. Firstly, we report a 61-year-old patient with partial oculomotor nerve palsy and contralateral cerebellar ataxia who demonstrated an infarction just caudal to the red nucleus on MRI. Secondly, we also discuss the probable vertical fascicular arrangement of the oculomotor nerve in the midbrain.
Brain Stem Infarctions*
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Cerebellar Ataxia
;
Humans
;
Infarction
;
Magnetic Resonance Imaging
;
Mesencephalon*
;
Middle Aged
;
Oculomotor Nerve
;
Oculomotor Nerve Diseases
;
Red Nucleus
8.Erosive Adenomatosis of the Nipple.
Hoon HUR ; Eui Chul JEONG ; Chang Woo LEE ; Joong Hwan KIM
Korean Journal of Dermatology 1986;24(4):541-543
We experienced a case of erosive adenomatosis of the nipple (EAN) in a 20-year-old lady. She have had an eczematous, erosive and crusted nipple, on the right si.de, with a serosanguineous discharge for the past two years. The biopsy specimen of eczematous lesion on the affected nipple showed focal erosion and acanthosis in the epidermis. Florid intraductal epithelial proliferation and solid nests were scattered in the nipple stroma without showing any cellular pleomorphism. The lining epithelium maintained two layers of cells the inner colurnnar cells and the outer cuboidal cells. Chronic inflammatory infiltrates of relatively dense lymphohisiocytes were found in the surrounding stromal tissue, Paget cells or underlying malignancy were not seen, and a group of tumor netst was confined to the upper part of the subareolar tissue.
Biopsy
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Epidermis
;
Epithelium
;
Humans
;
Nipples*
;
Young Adult
9.Auricular Reconstruction in Microtia Patients: A Single Institution Experience
Young Kyun HUR ; Yeonsu JEONG ; Sung Huhn KIM
Korean Journal of Otolaryngology - Head and Neck Surgery 2022;65(6):319-327
Background and Objectives:
Microtia is a congenital deformity where the pinna and middle ear structures are underdeveloped. Auricular reconstruction in microtia is one of the most difficult surgeries in otolaryngology due to the complex three-dimensional structure of the auricle. This study investigated the post-operative results in total auricular reconstruction performed by otologic surgeons in a single institution.Subjects and Method We analyzed data from 27 microtia patients who underwent auricular reconstruction in our institution from 2011 to 2019. The post-operative results were evaluated in terms of the shape of the auricle, the symmetry of the ear, and the degree of auriculocephalic sulcus stricture. The type and frequency of post-operative complications associated with the reconstruction were also evaluated.
Results:
Of the 24 patients, the shape of the auricle was good in 11 (40.7%), moderate in 11 (40.7%), and poor in 5 (18.6%) patients. The symmetry of the ear size was symmetric in 24 (88.9%) and asymmetric in 3 (11.1%) patients. The degree of auriculocephalic sulcus stricture was good in 11 (40.7%), partial stricture in 12 (44.4%), and severe stricture in 4 (14.8%) patients. Postoperative complications included skin necrosis, suture material exposure, and wound infection with cartilage deformation.
Conclusion
Total auricular reconstruction is a complex and sophisticated operation utilizing either autologous rib cartilage or artificial implant material. Considering that microtia is often accompanied by ear canal stenosis and hearing impairment, otolaryngologists should be more interested in the field of auricular reconstruction.
10.Diagnostic Value of Immediate CT after Chemoembolization in Patients with Hepatocellular Carcinoma: Comparison with 2-3 Week Delayed CT.
Yong Hoon KIM ; Jong Hoon KIM ; Soon Joo CHA ; Gham HUR ; Myeong Seok JEONG ; Jeong Joo WOO ; Jeong Wook SEO ; Jeong Hyeok KIM
Journal of the Korean Radiological Society 1995;33(2):247-251
PURPOSE: Lipiodol CT is a important modality for the diagnosis of hepatocellular carcinoma and compared is usually performed at 2-3 week after Lipiodol injection. Therefore, we assessed and the diagnostic value and merits of immediate CT after chemoembolization from there of 2-3 week delayed Lipiodol CT. MATERIALS AND METHODS: Thirty three cases of chemoembolization which were performed both immediate CT after chemoembolization and 2-3 week delayed Lipiodol CT were reviewed retrospectively. They were divided into four grades according to pattern of lipiodol uptake by three radiologists. The diagnostic value of immediate Lipiiodol CT was compared to delayed Lipiodol CT. RESULTS: Grade 0 was two cases(3.0%) and Grade 1 was seven cases(21.2%). In the cases of Grade 2(23/33, 69.7%) tumor uptake could be dishng wished from parenchymal uptake of Lipiodol by its density and pattern. Tumor uptake showed dense and homogeneous pattern, but parenchymal uptake revealed less dense and hepatoram-like wedge shaped pattern. Lipiodol uptake of tumor in Grade 3(1/24, 3.0%) was equal to that in delayed Lipiodrl CT. Grade 3 and 2(72.7%) of the immediate Lipiodol CT were not inferior to delayed Lipiodol CT in its diagnostic value. CONCLUSION: The immediate Lipiodol CT could make rapid establishment of treatment plan and are expected to be more convenient than delayed CT for the patients.
Carcinoma, Hepatocellular*
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Diagnosis
;
Ethiodized Oil
;
Humans
;
Retrospective Studies