1.Phakomatosis Pigmentovascularis Associated with Pyogenic Granuloma as well as Sturge-Weber Syndrome and Klippel-Trenaunay Syndrome.
Kyung Dal KIM ; Kyung Dal KIM ; Mu Hyoung LEE
Annals of Dermatology 2002;14(3):158-160
A 21-year-old Korean male was referred to our department in June, 1999 for the evaluation of extensive reddish patches and gray-bluish pigmentation since birth. Physical examination revealed two kinds of patches over the various parts of the body. Reddish patches suggesting nevus flammeus were located on the left side of face, chest, and both upper and lower extremities. Gray-bluish pigmented patches suggesting nevus of Ota were found on both the periorbital areas. A 0.5×0.6 cm erythematous papule was found on the right anterior chest. The results of its histopathologic examination were compatible with pyogenic granuloma. We made the diagnosis of phakomatosis pigmentovascularis associated with pyogenic granuloma as well as Sturge-Weber syndrome and Klippel-Trenanunay syndrome.
Diagnosis
;
Granuloma, Pyogenic*
;
Humans
;
Klippel-Trenaunay-Weber Syndrome*
;
Lower Extremity
;
Male
;
Neurocutaneous Syndromes*
;
Nevus of Ota
;
Parturition
;
Physical Examination
;
Pigmentation
;
Port-Wine Stain
;
Sturge-Weber Syndrome*
;
Thorax
;
Young Adult
2.A Case of Tubular Apocrine Adenoma.
Nack In KIM ; Tuk Woo LIM ; Kyung Dal KIM ; Nack In KIM
Annals of Dermatology 2002;14(2):102-105
Tubular apocrine adenoma(TAA) is a rare benign neoplasm usually found on the scalp. It has been designated as an apocrine histogenesis on the basis of its ultrastructural characteristics, enzyme, and immunohistochemical phenotype. Histopathologically the neoplasm consists of tubules or cysts, which show signs of apocrine secretion and sometimes needs to be differentiated from papillary eccrine adenoma. We report a typical case of TAA on nostril which shows differentiation toward apocrine in nature.
Adenoma*
;
Phenotype
;
Scalp
3.Meniscus Repair using Meniscus Arrow: Preliminary Report.
Kyung Taek KIM ; Sung Keun SOHN ; Dal Hee KIM
Journal of the Korean Knee Society 1998;10(1):73-77
No abstract available.
4.Clinical and Histopathologic Study of Eosinophilic Cellulitis.
Eun Kyung KIM ; Chan Keum PARK ; Jung Dal LEE
Korean Journal of Pathology 1995;29(3):334-342
Eosinophilic cellulitis is a rare dermatosis originally described by Wells as "recurrent granulomatous dermatitis with eosinophilia", then called Wells' syndrome. The etiology is unknown, although a hypersensitivity mechanism is suspected. Flame figures are considered as a characteristic histologic feature of Wells' syndrome. To clarify the nature of eosinophilic cellulitis and its flame figures, the authors have reviewed five cases of eosinophilic cellulitis with its clinical and histopathologic findings. Cutaneous lesions were variable in appearance and was confused with angioedema, urticarial vasculitis, erydiema multiforme, morphea or granuloma annulare. Microscopically, early lesions (2-7 days) showed diffuse dermal eosinophilic infiltration with widespread degranulation, sometimes extended into the underlying muscle. Subepidermal bulla was present in one case. Subsequently, granulomatous features with characteristic "flame figures" became apparent (several months). Collagen alteration by eosinophilic granules resulted in flame figure formation and a granulomatous response. In two patients, there were possible relationships between drug and flare-ups of eosinophilic cellulitis, but the others, no contributory precipitating factors were found. We think that eosinophilic cellulitis represents a severe anaphylactic hypersensitivity reaction to various stimuli showing characteristic histopathology with recurrent episodes and frequent hypereosinophilia in the peripheral blood.
5.Subcutaneous Neuromuscular Hamartoma: A case report.
Dong Hoon KIM ; Eun Kyung HONG ; Jung Dal LEE
Korean Journal of Pathology 1999;33(1):62-64
Subcutaneous form of neuromuscular hamartoma is extremely rare and histologically different from the conventional neuromuscular hamartoma of the peripheral nerve or benign Triton tumor by an indistinct nodular growth with ill-defined margin and marked collagen interposition. It is usually not associated with a major nerve. We report a case of subcutaneous neuromuscular hamartoma developed in the forehead of 24-year-old man. The tumor showed proliferation of dense, hyalinized fibrous tissue, in which single or group of mature skeletal muscle fibers and nerve fibers were haphazardly intermixed. Recognition of abnormally arranged muscle and nerve fibers is important not to miss this lesion.
Collagen
;
Forehead
;
Hamartoma*
;
Humans
;
Hyalin
;
Muscle Fibers, Skeletal
;
Neptune
;
Nerve Fibers
;
Peripheral Nerves
;
Skin
;
Young Adult
6.Morphometric Analysis of Malignant Lymphoma.
In Sook KIM ; Eun Kyung HONG ; Jong Dal LEE
Korean Journal of Pathology 1990;24(2):128-136
Nuclear morphology and size are important in the diagnosis and classification of non-Hodgkin's lymphoma. The recognition of morphologic features of the lymphoma cells and their interpretation are somewhat subjective and often difficult. We apply the morphometric study in touch imprints from 22 cases of non-Hodgkin's lymphoma classified by Working formulation. Determination of the exact size of the tumor cells and substantial diagnostic value of this method compared with histology are proposed. Morphometric parameters, including nuclear area, perimeter, maximal diameter (D-max), diameter of an equivalent circle for a measured area (D-circle), circularity factor (From PE) and regularity factor (Form AR) are measured, using Kontron, user-controlled image analyser (IBAS-1). The correlation between morphometric and histologic diagnosis is relatively good, except for 2 cases of Burkitt's lymphoma, measured as large cell and 2 cases of large cell lymphoma measured as medium cell. The most reliable parameter of the nuclear size is D-circle. The parameters for the nuclear shape, Form PE and Form AR, also reflect the nuclear cleavage and polymorphous pattern. The large cell group shows more wide standard deviation than small and medium cell groups, reflecting heterogeneity and variability in unclear size of large cell group. We suggests the morphometric analysis using touch imprints is complementary diagnostic tool for more accurate and reproducible diagnosis.
7.Gastric Choriocarcinoma and Endodermal Sinus Tumor in Collision Tumor.
Eun Kyung KIM ; Eun Kyung HONG ; Kwang Soo LEE ; Jung Dal LEE
Korean Journal of Pathology 1992;26(4):405-410
Both primary choriocarcinoma and endodermal sinus tumor of the stomach are very rare entities. Combination of these two tumors is even rarer, and only a single such case has been reported in English literature. The case had gastric adenocarcinoma in addition to these tumors. We experienced a case of combined, pure choriocarcinoma and endodermal sinus tumor in the stomach of a 74 year-old man. He had no gonadal or any other primary tumor. Huge exophytic tumor was located in the lesser curvature of the body. Two components of the tumor was separated and clearly defined. Human chorionic gonadotropin(HCG) was demonstrated in serum and in tissue sections. Alpha-fetoprotein(alpha-FP) was also demonstrated in serum and in tissue sections. Alpha-fetoprotein(alpha-FP) was also elevated in the serum. Possible tumor origin was speculated.
Humans
;
Adenocarcinoma
8.Cytologic features of glassy cell carcinoma of the uterine cervix.
Gu KONG ; Eun Kyung KIM ; Eun Kyung HONG ; Jung Dal LEE
Korean Journal of Cytopathology 1991;2(1):62-66
Glassy cell carcinoma is an unusual neoplasm of the uterine cervix with highly aggressive clinical behavior. On cervico-vaginal smear examination, the tumor has well confused of atypical repair cell of the endocervix. Recently, we have experienced two cases of glassy cell carcinoma of the uterine cervix, diagnosed on cervico-vaginal smears and confirmed on following histologic sections. The cervico-vaginal smears revealed abundant clusters with well defined boarders. The cell clusters were composed of large tumor cells. The tumor cells had distinct granular cytoplasm and eosinophilic macronucleoli. Characteristic cytologic features of this tumor were discussed in view of differential diagnosis.
Cervix Uteri*
;
Cytoplasm
;
Diagnosis, Differential
;
Eosinophils
;
Female
9.In vitro platelet assessment of the stored CPDA-1 platelet concentrates.
Kan Hee HAN ; Jang Soo SUN ; Nam Kyung KIM ; Jay Sik KIM ; Dal Hyo SONG
Korean Journal of Blood Transfusion 1992;3(2):143-150
No abstract available.
Blood Platelets*
10.Value of modified foley catheter method in the removal of blunt esophageal foreign bodies.
Kyung In KIM ; Yoo Mi CHA ; Heon HAN ; Dal Mo YANG ; Hyung Sik KIM ; Young Seok LEE
Journal of the Korean Radiological Society 1993;29(4):844-848
Removal of blunt esophageal foreign bodies using Foley catheter under a fluoroscopic guidance is a well-recognized procedure. However, since this procedure is rather cumbersome and uncomfortable to the patient, the authors tried to find an easier and more convenient modified technique. For 10 patients with esophageal foreign body, we tried the method to the patients who is lying in the right lateral decubitus position and 3 assistants hold head. arms, trunk and legs of the patients without tilting the table and without using immobilizer. Foley catheter is inserted through nostril, nasal cavity and pharynx to esophagus. In order to identify the Foley catheter in esophagus, 0.025 inch short wire was inserted in the Foley catheter. The balloon of a Foley catheter was inflated by 10cc of air, and the syringe was kept attached to the Foley catheter during the procedure. After passage of the foreign body through the upper esophageal sphincter, the balloon was deflated immediately and the foreign body was removed through the mouth. We successfully removed in removing all the blunt esophageal foreign body with ease. This modified method is also fast, safe and efficient.
Arm
;
Catheters*
;
Deception
;
Esophageal Sphincter, Upper
;
Esophagus
;
Foreign Bodies*
;
Head
;
Humans
;
Leg
;
Methods*
;
Mouth
;
Nasal Cavity
;
Pharynx
;
Syringes