1.Histopathologic Resemblance of Ovarian Dermoid Cyst to Various Skin Tumors.
Sun Wook HWANG ; Kwang Min LEE
Annals of Dermatology 1995;7(2):165-168
BACKGROUND: The wall of ovarian dermoid cysts shows various kinds of morphologic patterns. Some of them resemble the features of epidermal and epidermal appendageal tumors. OBJECTIVE: The purpose of this study is to classify the morphologic features of the wall of ovarian dermoid cyst from the dermatohistopathologic viewpoint. METHODS: H&E stained slides of 203 ovarian dermoid cysts were reviewed RESULTS: Thirteen different patterns of morphologic features were found. They included features of organoid nevus, sebaceous hyperplasia, steatocystoma multiplex, epidermoid cyst, nevus comedonicus, epidermal nevus, apocrine hidrocystoma, syringoma and trichilemmal cyst. CONCLUSION: Various epidermal and epidermal appendageal tumors may be associated with ovarian dermoid cyst.
Dermoid Cyst*
;
Epidermal Cyst
;
Female
;
Hidrocystoma
;
Hyperplasia
;
Nevus
;
Organoids
;
Ovary
;
Skin*
;
Steatocystoma Multiplex
;
Syringoma
2.Three cases of atypical Kawasaki disease with coronary aneurysm.
Min Young PARK ; Kwang Sun HAN ; Sung Yoon CHO ; Byoung Soo CHO ; Sung Ho CHA
Journal of the Korean Pediatric Society 1993;36(9):1315-1319
Kawasaki disease is described by fever lasting five days or more, bilateral conjunctival injection, changes of lips and oral cavity, polymorphous exanthema, acute non-purulent cervical lymphadenopathy, and changes of extremities. Atypical Kawasaki disease is defined as fewer than 4 of 6 criteria described above including coronary artery abnormalities. Especially, atypical clinical manifestations of Kawasaki disease appear in infants younger than 6 months old of age. Thus we recommend echocardiography in early infancy who has prolonged fever in order to diagnose atypical Kawasaki disease and treat early. We have experienced three cases of atypical Kawasaki disease with coronary aneurysm who were admitted because of fever and revealed coronary aneurysm on echocardiography.
Coronary Aneurysm*
;
Coronary Vessels
;
Echocardiography
;
Exanthema
;
Extremities
;
Fever
;
Humans
;
Infant
;
Lip
;
Lymphatic Diseases
;
Mouth
;
Mucocutaneous Lymph Node Syndrome*
3.Flow cytometric DNA analysis of gastric cancer--correlation with histology and clinical outcome.
Journal of Korean Medical Science 1993;8(5):348-354
Nuclear DNA content was analysed by means of flow cytometric measurements in 103 patients with gastric carcinomas, using paraffin-embedded archival tissue. DNA aneuploidy was found in 40 cases (38.8%). The mean DNA index of aneuploid tumors was 1.45(range 1.13 to 2.37). No significant association between ploidy and either age, sex, tumor location, size, stage, growth pattern, or histologic type was found. However, the incidence of aneuploidy was higher in high grade carcinomas than in low grade carcinomas; the incidence of aneuploidy was 10%, 68.8%, and 45.8% for Grade II, III, and IV carcinomas, respectively, as compared with Grade I carcinomas which were all diploid. On statistical analysis, Abnormal cellular DNA content was significantly correlated with high histologic grade (P<0.005). Patients with aneuploid cancer (39.2%) had a poorer prognosis than those with diploid cancer (70.0%) based on (P<0.01). The 2-year survival rate for advanced gastric carcinoma. Therefore, DNA ploidy might be a useful prognostic factor in cases of advanced gastric cancer.
Adult
;
Aged
;
Aneuploidy
;
DNA, Neoplasm/*analysis
;
Female
;
*Flow Cytometry
;
Follow-Up Studies
;
Humans
;
Male
;
Middle Aged
;
Stomach Neoplasms/*genetics/pathology
4.Atypical Mesoblastic Nephroma: Report of a case.
Jin Man KIM ; Dong Wook KANG ; Seung Ki MIN ; Kwang Sun SUH ; Dae Young KANG
Korean Journal of Pathology 1991;25(6):601-606
Congenital mesoblastic nephroma(CMN) is an important differential diagnosis of a renal mass occurring in the newborn or in early childhood. It was first described by Bolande as a separate disease entity distinct form Wilms' tumor. In 1974, Beckwith has predicted that this tumor has a pathologic spectrum with classic congenital mesoblastic nephroma at one extreme, unequivocally mallignant spindle cell sarcomas at the other, and intermediate "gray zone" lesions of indeterminate biologic significanse. In 1986, Joshi has described "atypical mesoblastic nephroma" as a potentially aggressive variant of CMN, which shows atypical gross and microscopic features such as hemorrhage, necrosis, high cellularity, and mitotic index. We report of a case of atypical mesoblastic nephroma presenting in a 38 days-old male infant. Grossly, the tumor involved the upper and midportion of the left kidney. On section, the cut surface was fleshy, grayish-white, and homogeneous. Microscopically, the tumorshowed high degree of cellularity and arrangement of fusiform cells in sheets and vague interlacing bundles. The individual tumor cells showed fusiform to oval nuclei, indistinct scanty pale-eosinophilic cytoplasm and many mitotic figures.
Infant
;
Child
;
Male
;
Female
;
Infant, Newborn
;
Humans
;
Diagnosis, Differential
5.Neuroendocrine Carcinoma of the Gallbladder Arising as Double Tumor.
Dae Hyun BAEK ; Seong Ki MIN ; Jin Man KIM ; Kwang Sun SUH ; Dae Young KANG
Korean Journal of Pathology 1990;24(3):299-303
Pleomorphic (undifferentated) carcinoma is a rare histologic type of carcinomas of the gallbladder and an atypical carcinoid is thought to be an intermediated type between carcinoid tumor and small cell carcinoma. Dense core "neurosecretory" granules can be found in the above mentioned tumors. We experienced a case of a double tumor of the gallbladder in a 51-year old male patient. Grossly, a large solid mass, about 5.0 cm in diameter, was found in the fundic portion and the neck portion also had a small 1.5 cm-sized polypoid mass. Microscopically, these lesions had features of pleomorphic carcinoma and atypical carcinoid, respectively. Immunohistochemically, they manifested reactivity for neuron specific enolase. Ultrastructural study revealed neurosecretory granules in the cytoplasms of tumor cells of the fundic and neck masses. Although light microscopic features of these tumor masses are quite different, we consider that these tumors represent a spectrum of neuroendocrine differentiation.
Male
;
Humans
6.Epidermal Nevus Syndrome with Various Skin Manifestations.
Kyu Kwang WHANG ; Seung Min LEE ; Eun Sun CHOI ; Yoon Kee PARK
Annals of Dermatology 1993;5(1):56-59
We report a case of epidermal nevus syndrome showing various skin manifestations improved with CO₂ laser and chemical peeling in a 11-year-old girl. Skin lesions were composed of linear verrucous plaques and numerous papillomatous papules on the face, neck, scalp and trunk, multiple congenital nevocellular nevi on the face, and extensive cafe au lait spots on the trunk. The associated findings of skeletal involvement were gingival hemihypertrophy and benign bone lesion of the 7th rib. CO₂ laser and chemical peeling MCA, 50% TCA) were applied to remove these skin lesions which improved considerably.
Cafe-au-Lait Spots
;
Child
;
Female
;
Humans
;
Neck
;
Nevus*
;
Ribs
;
Scalp
;
Skin Manifestations*
;
Skin*
7.Epidermal Nevus Syndrome with Various Skin Manifestations.
Kyu Kwang WHANG ; Seung Min LEE ; Eun Sun CHOI ; Yoon Kee PARK
Annals of Dermatology 1993;5(1):56-59
We report a case of epidermal nevus syndrome showing various skin manifestations improved with CO₂ laser and chemical peeling in a 11-year-old girl. Skin lesions were composed of linear verrucous plaques and numerous papillomatous papules on the face, neck, scalp and trunk, multiple congenital nevocellular nevi on the face, and extensive cafe au lait spots on the trunk. The associated findings of skeletal involvement were gingival hemihypertrophy and benign bone lesion of the 7th rib. CO₂ laser and chemical peeling MCA, 50% TCA) were applied to remove these skin lesions which improved considerably.
Cafe-au-Lait Spots
;
Child
;
Female
;
Humans
;
Neck
;
Nevus*
;
Ribs
;
Scalp
;
Skin Manifestations*
;
Skin*
8.Analysis of Octyl-2-Cyanoacrylate as a Dressing Material after Pediatric Urological Procedures.
Hahn Ey LEE ; Sun Ho MIN ; Kwang Myung KIM
Journal of the Korean Society of Pediatric Nephrology 2012;16(2):115-120
PURPOSE: We aimed to evaluate the efficacy of Octyl-2-cyanoacrylate (Dermabond(TM)) as a topical skin adhesive for pediatric urologic open surgery. METHODS: From August 2010 to August 2011, we retrospectively evaluated pediatric patients who underwent urologic open surgery at our institution. A total of 128 pediatric patients with 210 incisions used Dermabond(TM) for skin closure. RESULTS: We divided the 128 patients into 3 groups according to type of surgery. Group 1 underwent hydrocelectomy (55 cases, 41.3%), Group 2 underwent orchiopexy (43 cases, 32.3%), Group 3 underwent penoplasty (35 cases, 26.4%). One hundred and twenty eight patients who underwent 133 surgeries in total, with a total of 210 incisions visited our outpatient department postoperatively, and a total of 5 wound complications (2.3%) occurred, but were simple inflammations and no dehiscence was observed. When analyzed according to groups, no wound problems occurred in Group 1 (0/55, 0%), one occurred in Group 2 (1/43, 2.3%) and four cases occurred in Group 3 (4/35, 11.4%) respectively. When re-analyzed according to wound locations, one occurred in an inguinal wound (1/120, 0.83%), none occurred in scrotal wounds (0/55, 0%), and four occurred in penile wounds (4/35, 11.4%). In Group 3, the incidence of penile wounds was significantly increased compared to other groups (P=0.008). All 5 wound problems were inflammatory and healed at an average of 13.8 days (13-15 days) with antibiotic ointment application only. CONCLUSION: Dermabond(TM) is feasible and safe topical skin adhesive alternative to standard skin suture in pediatric urologic surgery. However, further research about its efficacy and safety could be valuable in the future.
Adhesives
;
Bandages
;
Humans
;
Incidence
;
Inflammation
;
Male
;
Orchiopexy
;
Outpatients
;
Retrospective Studies
;
Skin
;
Sutures
;
Tissue Adhesives
;
Urologic Surgical Procedures
9.A Case of Pulmonary Blastoma.
Kang Seo PARK ; Kyu Sun CHOI ; Kyong Nyong KIM ; Wan Soeb KIM ; Kwang Min LEE ; Dong Kyu CHUNG
Journal of the Korean Pediatric Society 1990;33(10):1447-1453
No abstract available.
Pulmonary Blastoma*
10.An Atypical Case of Aicardi Syndrome with Favorable Outcome.
Seung Woo LEE ; Kwang Soo KIM ; Sung Min CHO ; Sun Joo LEE
Korean Journal of Ophthalmology 2004;18(1):79-83
Aicardi syndrome is a severe congenital disorder characterized by infantile spasms, chorioretinal lacunae, and agenesis or hypogenesis of the corpus callosum. A 6 month old female had developed abnormal eye movement and seizures of the complex partial type and myoclonic type. MRI pictures of the patient revealed the presence of genu associated with agenesis of the rest of corpus callosum. A funduscopic examination revealed bilateral small, solitary, pale areas with sharp borders, some of which had minimal surrounding pigmentation (chorioretinal lacunae), especially clustered around the disc, and they were more prominent on the left side. We report here on the unusual findings of a complex partial seizure, myoclonic seizure and the atypical EEG finding in addition to the well-known characteristic clinical and imaging findings of a patient with Aicardi syndrome.
Anticonvulsants/therapeutic use
;
Arachnoid Cysts/*pathology
;
Corpus Callosum/*abnormalities
;
Electroencephalography
;
Epilepsies, Myoclonic/drug therapy/*pathology
;
Epilepsies, Partial/drug therapy/*pathology
;
Female
;
Humans
;
Infant
;
Magnetic Resonance Imaging
;
Retinal Diseases/*pathology
;
Spasms, Infantile/drug therapy/*pathology
;
Syndrome