1.A Case of Skin Tag like Preaxial Polydactyly.
Heun Jung CHO ; Dong Kun KIM ; Dong Sik BANG
Korean Journal of Dermatology 1997;35(2):379-382
Polydactyly is the most common congenital anomaly of the upper limb. Polydactyly is classified as preaxial polydactyly(thumb), central polydactyly(index, middle and ring fingers), and postaxial polydactyly(little finger) by the site of the extra digit. A 3-day-old female newborn had a 1.5 * 1.0cm sized flesh color ed pedunculated sac like mass on the proximal phalanx of her right thumb since birth. A roentgenogram on the hand revealed no bony abnormalities of the digit and the mass contained no bony structures. The stalk of the mass was cut by the CO2 laser. On histopathological examination, a cartilage structure was found in the loosely arranged, edematous dermis and the overlying epidermis was flattened. The clinical and histological findings support the diagnosis of preaxial polydactyly. We report this interesting case of preaxial polydactyly with a review of the literature.
Cartilage
;
Color
;
Dermis
;
Diagnosis
;
Epidermis
;
Female
;
Hand
;
Humans
;
Infant, Newborn
;
Lasers, Gas
;
Parturition
;
Polydactyly*
;
Skin*
;
Thumb
;
Upper Extremity
2.An Unusual Case of Acinic Cell Tumor.
Hae Eul LEE ; Dong Sik BANG ; Jung Bock LEE
Korean Journal of Dermatology 1983;21(2):243-247
Acinic cell tumor, a rare tumor of the salivary gland origin, consists of cells similar to the serous cells of the salivary gland. The tumor is almost exclusively paroti4 gland origin, accounting for 2. 7 to 4. 0% of all parotid tumors. The tumor is not,benign but has at least a low-grade malignant potential. We described herein a case of acinic cell tumor which had occurred on an unusual site, right inner epicanthal area of a 9-year-old girl Microscopically, a hematoxylin-eosin stained biopsy specimen showed rnany lobules com of round or polyhedral tumor cells. Each tumor cell had distinct cell membrane, clear cytoplasm, and relative1y eccentric nucleus. The cytoplasm of tumor cell cantaine4 diastase resistant PAS-positive material.
Acinar Cells*
;
Amylases
;
Biopsy
;
Carcinoma, Acinar Cell*
;
Cell Membrane
;
Child
;
Cytoplasm
;
Female
;
Humans
;
Salivary Glands
3.Family's burden of psychotic in-patient.
Jung Sik LEE ; Kwang Iel KIM ; Dong Yul OH
Journal of Korean Neuropsychiatric Association 1991;30(3):517-531
No abstract available.
4.A Case of Giant Fibrous Histiocytoma.
Yoon Kee PARK ; Min Geol LEE ; Dong Sik BANG ; Tae Jung KWON ; Jung Sook KIM
Korean Journal of Dermatology 1984;22(1):83-88
Fibrous histiocytomas are characterized by a variable combination of cells with fibroblastic and histiocytic features. They exhibit a distinctive but inconstant cellular arrangement referred to as a storiform or cartwheel pattern. Considerable corfusion has enveloped these tumors as a result of their various terminology-fibrous histiocytoma, dermatofibroma, sclerosing hemangioma, fibroxanthoma, subepidermal nodular fibrosis, xanthogranuloma, giant cell tumor of tendon sheath. A histologically benign but locally infiltrating, 15 * 20cm sized, fibrous histiocytoma was found in the posterior aspect of left thigh of a 17-year-old man. The tumor was incompletely excised due to adhesion of the tumor mass to sciatic nerve and then radiation therpy was combined, Histogenesis and prognostic aspects of the tumor are discussed.
Adolescent
;
Fibroblasts
;
Fibrosis
;
Giant Cell Tumors
;
Histiocytoma
;
Histiocytoma, Benign Fibrous*
;
Humans
;
Sciatic Nerve
;
Tendons
;
Thigh
5.Two cases of squamous cell carcinoma arising from benign teratomaas of ovary.
Young Bae LEE ; In Sik LEE ; Young Tak KIM ; Dong Geun JUNG ; Ahm KIM ; Jung Eun MOK
Korean Journal of Obstetrics and Gynecology 1992;35(8):1253-1258
No abstract available.
Carcinoma, Squamous Cell*
;
Female
;
Ovary*
6.Congenital Systemic Cytomegalic Inclusion Disease.
Dong Beom LEE ; Dong Hyun KIM ; Jung Sik MIN ; Chang Hee CHOI ; Je Geun CHI
Journal of the Korean Pediatric Society 1990;33(1):100-106
No abstract available.
Cytomegalovirus Infections*
7.The clinico-pathological study of the torsion of the uterine adnexa.
Hee Dong YANG ; Hyun Jik PARK ; Choong Sik HA ; Seon Je HWANG ; Jung Sang GWAK
Korean Journal of Obstetrics and Gynecology 1993;36(7):1470-1474
No abstract available.
8.Tuberculous Spondylitis: Contrast Enhanced MR Imaging.
Dong Ik KIM ; Choon Sik YOON ; Jung Ho SUH ; Sok Jong RYU
Journal of the Korean Radiological Society 1994;30(5):915-922
PURPOSE: This retrospective study was conducted to evaluate the value of adminstration of IV gadopentetate dimeglumine for MR imaging of tuberculous spondylitis. MATERIALS AND METHODS: The authors reviewed MR images both with and without contrast enhancement of 22 patients with tuberculous spondylitis. Evaluation of signal characteristics, enhancement patterns, and difference of delineation between pre- and postcontrast enhancement was made on 4 compartments the vertebral body, intervertebral disc, paravertebral space, and extradural space. RESULTS: The spinal tuberculous lesions revealed relatively low or isosignal intensity on T1-weighted image and high signal intensity on T2-weighted image. The tuberculous lesions of vertebral body showed enhancement of mixed pattern, and rim enhancement pattern was predominant in the other 3 compartment, suggesting abscess. The contrast enhanced MR image showed better demarcation of the extents of tuberculous lesions comparing with noncontrast image, especially at the vertebral body and intervertebral disc. The nature of tuberculous involvement was better visualized at the extradural space and paravertebral space on postcontrast image. CONCLUSION: We conclude Gd-DTPA enhanced MR image can give informations for more detailed delineation, extents, and nature of involvement in the tuberculous spondylitis.
Abscess
;
Gadolinium DTPA
;
Humans
;
Intervertebral Disc
;
Magnetic Resonance Imaging*
;
Retrospective Studies
;
Spondylitis*
9.A case of bronchial arterial embolization of massive hemoptysis.
Youn Sik LIM ; Jung Eun SUH ; Suk JEONG ; Dong Ill CHO ; Jae Won KIM
Tuberculosis and Respiratory Diseases 1991;38(4):396-400
No abstract available.
Hemoptysis*
10.Wegener' s Granulomatosis.
Soo Jung KIM ; Sang Hoon PARK ; Kwang Hoon LEE ; Dong Sik BANG ; Soo Kon LEE
Korean Journal of Dermatology 1995;33(6):1129-1133
Wegener's granulomatosis is a systemic necrotizing vasculitis of unknown cause. The disease is characterized by the involvement of the upper airway, the lung, and the kidney. Skin lesions are frequent and the most common lesion is purpura distributed on the limbs and trunk. A 34-year-old female showed recurrent purpuric macules on the both lower extremities and buttocks. The patient. showed nasal septal perforation with saddle nose deformity and C-ANCA positivity. Histopathologic findings of purpuric lesion revealed the features of necrotizing vasculitis. The histologic specimen from the nasal cavity showed chronic inflammation with granuloma formation and kidney showed focal necrotizing glomerulonephritis. Therefore, we treated the patient with prednisolone and cyclophosphamide having diagnosed Wegener's granulomatosis.
Adult
;
Antibodies, Antineutrophil Cytoplasmic
;
Buttocks
;
Congenital Abnormalities
;
Cyclophosphamide
;
Extremities
;
Female
;
Glomerulonephritis
;
Granuloma
;
Humans
;
Inflammation
;
Kidney
;
Lower Extremity
;
Lung
;
Nasal Cavity
;
Nasal Septal Perforation
;
Nose
;
Prednisolone
;
Purpura
;
Skin
;
Vasculitis
;
Wegener Granulomatosis