1.Giant Osteoma of the Anterior Cranial Fossa: Case Report .
Ki Seong EOM ; Tae Young KIM ; Jong Moon KIM
Journal of Korean Neurosurgical Society 2002;32(1):59-62
Osteoma is the most common benign tumor of the cranium, and the frontal sinus is its most frequent location in the cranium. A 39-year-old woman presented with left exophthalmos was found to have orbital and intracranial extension of a giant osteoma involving anterior cranial fossa. The etiology, presenting features, diagnosis and treatment of this tumor are reviewed.
Adult
;
Cranial Fossa, Anterior*
;
Diagnosis
;
Exophthalmos
;
Female
;
Frontal Sinus
;
Humans
;
Orbit
;
Osteoma*
;
Skull
2.Primary omental torsion: two cases.
Ki Boong KIM ; Sung Tae OH ; Yong Wha MOON
Journal of the Korean Surgical Society 1992;42(3):404-407
No abstract available.
3.Anatomical Investigation of Sural Nerve and Its Contributing Nerves.
Yoon Tae KIM ; Joo Sung MOON ; Joon Ki KIM
Journal of the Korean Academy of Rehabilitation Medicine 2003;27(5):723-726
OBJECTIVE: To identify the location and formation of the sural nerve and its contributing nerves. METHOD: Fourteen lower limbs of 7 adult cadavers were anatomically dissected. The location and formation of the sural nerve (SN) in relation to the medial sural cutaneous nerve (MSCN) and the lateral sural cutaneous nerve (LSCN) were investigated. The length and diameter of the SN and contributing nerves were measured and the differences of the results were analyzed. RESULTS: Twelve SNs were formed by the union of the MSCNs and LSCNs, and 2 SNs were direct extensions of the MSCNs. The point of formation of the SN by union of the MSCN and LSCN was found in the middle third of the legs in 66.7% of SNs examined. The union sites of the SNs were located at 40.58+/-13.97% of the length of lower leg from the tip of lateral malleolus and 55.84+/-6.48% of the calf width from the medial border of the calf. There were significant statistical differences of diameter among nerves (p<0.05) and no significant difference of length between MSCN and LSCN. CONCLUSION: The results of this cadaveric study would increase the accuracy of the sural nerve conduction study and provide the locational information for precise surgical approach.
Adult
;
Cadaver
;
Humans
;
Leg
;
Lower Extremity
;
Sural Nerve*
4.Formal charts for quantified Tc-DMSA renal uptake rates.
Tae Yong MOON ; Yong Ki KIM ; Su Hee HWANG ; Chong Byung YOON ; Kyung Tak SEUNG
Korean Journal of Nuclear Medicine 1993;27(2):248-255
No abstract available.
5.Malignant Neurocutaneous Melanosis: A Case Report.
Tae Young KIM ; Kwang Soo OH ; Young Jin LEE ; Ki Jung YUN ; Jong Moon KIM
Journal of Korean Neurosurgical Society 2000;29(3):389-395
No abstract available.
Melanosis*
6.Involucrin Expression in Epidermal Tumors.
Doo Chan MOON ; Myung Ki HYUN ; Kyung Sool KWON ; Tae Ahn CHUNG
Korean Journal of Dermatology 1989;27(2):145-156
Involucrin is a recently recognized structural component of mature squamous epithelial cells and is considered as a marker of normal eratinocyte differentiation and ma.turation. In this study peroxidase-antiperoxidase techniques were used to assess involucrin expression in histologic sections of normal skin and a variety of epidennal tumors including squamous cell carcinomas(25 cases), keratoacanthomas(11 cases), basal cell carcinomas(20 cases), trichoepitheliomas(5 cases), Howens diseases(12 cases), arsenic keratoses(10 cases), actinic keratoses(10 cases) and Pagets diseases(2 cases). The results were as follows : l. In normal skin, the upper third of the viable epidermis showed diffuse cytoplasmic staining for involucrin. In hair follicles, the lower area of inner root sheath and inner area of the outer root sheath stained positively. The sebareous glands did not stain, but the ducts of sebaceous glands were positive. 2. Keratoacanthomas showed a relatively homogeneous staining pattern for inirolucrin ', all cells except basal cells stained with mild to moderate intensity. In contrast, squamous cell carcinomas disclosed a highly irregular involucrin staining pattern with marked variation in staining intensity from cell to cell. 3. Basal cell carcinomas were negative for involucrin except squamous horn cysts, and the epidermis overlying basal cell carcinomas showed the field effect, that is, the epidermis overlying the tumors exhibited diffuse, homogeneous positive staining of cells in all layers of the epidermis. 4. ln trichoepitheliomas, the involucrin reactivity was negative as in basal cell carcinoma.s, but the field effect was not observed. 5. In Elowens disease, actinic keratosis, arsenic keratosis and Pagets disease, the positivit.y for involucrin staining extended deeper into the stratum malpighii than was observed wit,h normal epidermis. And areas showing irregular patchy pattern of involucrin staining were considered to have the potentiality of malignant invasive change much more than the negative or homogeneous areas. Paget's cells were negative for involucrin as the adjoining keratinocytes in the lower portion af epidermis.
Actins
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Animals
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Arsenic
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Carcinoma, Basal Cell
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Carcinoma, Squamous Cell
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Cytoplasm
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Epidermis
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Epithelial Cells
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Hair Follicle
;
Horns
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Keratinocytes
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Keratoacanthoma
;
Keratosis
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Keratosis, Actinic
;
Sebaceous Glands
;
Secobarbital
;
Skin
7.A Case of Collet-Sicard Syndrome Resulting from Jugular Vein Thrombosis.
Tae Sun MOON ; Ki Bum SUNG ; Dong Jin SHIN
Journal of the Korean Neurological Association 1994;12(2):348-353
Collet-Sicard syndrome is one of the syndromes of the multiple lower cranial nerve palsies, characterized by unilateral paralysis of 9th through 12th cranial nerves. The present report describes a 34-year-old woman who had hoarseness, dysarthria, and loss of taste developed after febrile illness. Brain MRI, both T1WI and T2WI, showed high signal intensity in the left jugular foramen. Gd-GTPA contrast injection revealed thickening and enhancement of the left tentorium. Angiography disclosed nonvisualization of the left transverse and sigmoid sinus, and reconstruction of the left internal and external jugular vein by collaterals from the angular, facial, and posterior fossa veins. The patient improved spontaneously two months later. This is the first report of Collet-Sicard syndrome resulting from jugular vein thrombosis.
Adult
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Angiography
;
Brain
;
Colon, Sigmoid
;
Cranial Nerve Diseases
;
Cranial Nerves
;
Dysarthria
;
Female
;
Hoarseness
;
Humans
;
Jugular Veins*
;
Magnetic Resonance Imaging
;
Paralysis
;
Thrombosis*
;
Veins
8.Significance of the Serum Levels of C - reactive Protein in Leprosy Patients with Planter Ulcer.
Myung Ki HYUN ; Doo Chan MOON ; Kyung Sool KWON ; Tae Ahn CHUNG
Korean Journal of Dermatology 1990;28(3):302-307
It is difficult to know whether the presence of infection in the plantar ulcer in patients with leprosy or not. Because routine bacteriology is often unhelpful, we need to investigate diagnostic method in this situation. C-reactive protein(CRF) levels have been known to be useful in detecting infection in some diseases. In this study, CRP levels were measured in 20 leprosy patients with plantar ulceration and 14 patients with leprosy alone. The results were as follows : 1. There was no elevation of CRP levels in patients with leprosy alone, and in the majority of patients with ulcers. 2. Of 20 patients with plantar ulcers, four had raised CRP levels one had clinically obvious infection, and three had erythematous skin of uncertain cause surrounding their ulcers. 3. Treatment with an appropriate antibiotics reduced CRP levels to normal, which was associated with clinical improvement. Therefore, it is suggested that increased CRP levels can be a useful probe for detecting significant bacterial infection in plantar ulcers of leprosy patients.
Anti-Bacterial Agents
;
Bacterial Infections
;
Bacteriology
;
Foot Ulcer
;
Humans
;
Leprosy*
;
Skin
;
Ulcer*
9.Pure Motor quadriplegia in Bilateral Medial Medullary Syndrome.
Tae Sun MOON ; Young Ki LEE ; Dong Jin SHIN
Journal of the Korean Neurological Association 1996;14(1):295-297
Medullary pyramid is the one place where corticospinal fibers are isolated as the pyramidal tract, and the result of such lesions has been a flaccid hemiplegia. Medial medullary syndrome may occur bilaterally, resulting in flaccid quadriplegia with facial sparing, bilateral lower motor neuron signs of the tongue, and complete loss of position and vibratory sensation affecting all for extremities. Occasionally, only the pyramid is damaged, resulting in a pure motor quadriplegia without other medullary signs. We report a 78-year-old man who suddenly developed flaccid quadriplegia without any other medullary signs. Brain MRI showed bilateral medial medullary infarctions that was probably due to anterior spinal artery occlusion.
Aged
;
Arteries
;
Brain
;
Extremities
;
Hemiplegia
;
Humans
;
Infarction
;
Magnetic Resonance Imaging
;
Motor Neurons
;
Pyramidal Tracts
;
Quadriplegia*
;
Sensation
;
Tongue
10.A Clinical Study on Neurofibromatosis Evaluation by Riccardi's Classification.
Myung Ki HYUN ; Doo Chan MOON ; Kyung Sool KWON ; Tae Ahn CHUNG
Korean Journal of Dermatology 1990;28(2):194-201
Clinical study on 62 patients (26 males and 36 females) with neurofibromatosis seen during past ten years at the Department of Dermatology, Pusan National Universitg Hospital, was made the variable clinical manifestations of the disease and Riccardis ciassification were emphasized. The results were as follows . 1) Family history was noted in 32 cases(51.6%) and exhibited autosomal dominant inheritance pattern. 2) Cutaneous neurofibromas were found in 52 cases(83.8%). 3) Cafe-au-lait spots, measuring greater than 1.5cm in its longest diameter, were found in 60 cases(96.8%) and 44 cases(71.0%) had more than 6 in number. 4) Among associated abnormalities were,' mental retardation(20,9%), skeletal abnormalities(11.2%), seizure, severe headache, etc. 5) According to Riccardis classification, 38 cases could be classified as type I, 28 cases(73.7%); type II, 0 case ; type III, 1 case(2.6%); type IV, 3 cases(7, 9%); type V, 1 case(2.6%); type VI, 4 cases(10.5%); type VII, l case(2.6%); and type VIII, 0 case.
Busan
;
Cafe-au-Lait Spots
;
Classification*
;
Dermatology
;
Headache
;
Humans
;
Inheritance Patterns
;
Male
;
Neurofibroma
;
Neurofibromatoses*
;
Seizures