Intracranial nerve sheath tumors unrelated to the cranial nerve roots are extremely rare, and the origin of the tumors are debatable. We report a case of pathologically-proven neurofibroma inside the lateral ventricle. A 49-year-old man presented with headache of 6 months duration, urinary incontinence, visual disturbance and right hemiplegia. Brain CT scan showed a well defined isodense mass with homogenous contrast enhancement and marginal calcification. At surgery the tumor was found to be a 4cm-sized lobulated mass attached only to the choroid plexus. Histologically, the tumor masses consisted of fasciculating bundles of wavy spindle cells, with a considerable collagen laydown.
Brain ; Choroid Plexus ; Collagen ; Cranial Nerves ; Headache ; Hemiplegia ; Humans ; Lateral Ventricles ; Middle Aged ; Nerve Sheath Neoplasms ; Neurofibroma* ; Tomography, X-Ray Computed ; Urinary Incontinence

Castleman's disease is a benign disorder characterized by hypervascular lymphoid hyperplasia. The etiology of the disease is still unknown. Although it may occur at the various sites such as peritoneum, retroperitoneum, pelvic lymph node, muscle and lung, it occurs most commonly at the mediastinum. Even though specific pathophysiologic relations are still not clearly determined between two different histologic types -hyaline vascular type and plasma cell type-, there were several previous reports dealing with the plasma cell type transformed or progressed into different types of malignancies such as malignant lymphoma, Kaposi's sarcoma and Hodgkin's disease. We experienced a case of plasma cell type Castleman's disease that transformed into a malignant lymphoma and report this case with review of literatures.
Giant Lymph Node Hyperplasia* ; Hodgkin Disease ; Hyperplasia ; Lung ; Lymph Nodes ; Lymphoma* ; Mediastinum ; Peritoneum ; Plasma Cells* ; Plasma* ; Sarcoma, Kaposi

BACKGROUND: This study is aimed to elucidate the developmental pattern of human fetal lip by histological and immunohistochemical examinations. METHODS: Totally 231 normal human lip tissues obtained from autopsied fetuses were fixed with 10% buffered formalin, sectioned in cross and longitudinal directions, routinely stained for H&E and performed for immunohistochemistry with antibodies of S-100 protein, proliferating cell nuclear antigen (PCNA), transglutaminase C (TGase-C), metalloproteinase (MMP)-3, MMP-10, tenascin, KL1, K8.12, E-cadherin, tissue inhibitors of matrix metalloproteinase (TIMP)-1, TIMP-2 and total keratin (TK). RESULTS: The lip structure first appeared as an orifice of stomodeum around the 7-8th week of gestation, and a major structure of the midface was observed by the 11-12th week. As the squamous epithelium of the lip became thick and was keratinized, the vermilion border became distinguished in the 15-16th week, and the lip structure was almost completed with the presence of orbicularis oris muscle in the lingual side of vermilion border by the 17-18th week. Immunohistochemically, the vermilion border showed strong reactions for tenascin, E-cadherin and MMP-3 and increased positivity for PCNA, cytokeratins (TK, KL1, K8.12), and TGase-C. CONCLUSIONS: With the above findings we suppose that the cytodifferentiation of vermilion border epithelium plays an important role for the development of human fetal lip.
Antibodies ; Cadherins ; Epithelium ; Fetus ; Formaldehyde ; Humans* ; Immunohistochemistry ; Keratins ; Lip* ; Pregnancy ; Proliferating Cell Nuclear Antigen ; S100 Proteins ; Tenascin ; Tissue Inhibitor of Metalloproteinase-2

Fingerprints have been used for personal identification, for revealing physical anthropological characteristics, and for diagnosing genetic disorders. Morphology of fingerprints has been analyzed in various tribes. However, in Korean, the analytical methods of fingerprints and the numbers of subjects were not sufficient to find standard values for Korean fingerprints. In this study, fingerprints of 3216 Koreans (2095 males and 1121 females) were analyzed using the various methods and compared with those of other tribes to contribute in revealing physical anthropological characteristics of Korean and also in diagnosing genetic disorders of Korean. The results were as follows. 1. The incidence of ulnar loop type, whorl type, radial loop type, and arch type was 50.4%, 42.9%, 3.8%, and 2.9%, respectively. Data from the comparison of the incidences of fingerprint types in Korean with those in various tribes lead us to conclude that Korean belongs to the Asians and becomes closer to the Whites and Blacks in which loop type is frequent and whorl type is not frequent. 2. Fingerprint type seems to be related to the strength of finger since whorl type was frequent in male and in right hand, and arch type was frequent in female and in left hand. In addition, loop of fingerprint appears to have the tendency to open to the side bearing more physical contact since radial loop type was frequent in second finger, and ulnar loop type was frequent in fifth finger. 3. Among the subtypes of fingerprint, morphologically simple types were common. Among the subtypes of arch types, simple arch type with the same number of radial dermal ridges as ulnar ones was the most common. Among the subtypes of loop types, ulnar loop type without concentric circles or spirals was the most common. Among the subtypes of whorl types, concentric whorl type without loops was the most common. 4. Finger ridge counts were 16.9, 13.9, 11.9, 11.3, and 11.2 in first, fourth, third, second, and fifth finger, respectively; and were greater in male than in female. Finger ridge counts are greater in fingers which shows whorl type. However, there would be other factors to determine finger ridge counts; for examples, the size and behavioral habit of finger.
African Continental Ancestry Group ; Asian Continental Ancestry Group ; Dermatoglyphics* ; Female ; Fingers ; Hand ; Humans ; Incidence ; Male ; Population Groups

1. The intracranial pressure (ICP) was raised by the extradural balloon method in urethane-anesthetized rabbits, and change of the arterial blood pressure (BP) with change of ICP was studied. 2. In the control rabbit group raising ICP resulted in marked increase in BP. 3. In the reserpine-treated group raising ICP did not induce the increase in BP but the decrease in BP. 4. In the tetrabenazine-treated group raising ICP did not cause change in BP. 5. After the administration of norepinephrine through the lateral ventricle to the reserpine-treated and tetrabenazine-treated rabbits, raising ICP resulted in marked increase in BP. 6. These results indicate that the existence of norepinephrine in the brain is essential for the BP increase by raising ICP.
Arterial Pressure ; Blood Pressure* ; Brain* ; Intracranial Pressure* ; Lateral Ventricles ; Norepinephrine* ; Rabbits

OBJECTIVE: In order to elucidate the retrogressive degeneration of orofacial cleft, the fissured tissues of prenatal and postnatal cleft lip and palate were examined by histological and immunohistochemical methods. DESIGN: Totally 42 cases of prenatal (n=17) and postnatal (n=25) cleft lip and/or palate were examined in comparison with 10 cases of normal lip and oral mucosa using immunohistochemical stainings of MMP-3, MMP-9, MMP-10, cathepsin G, PCNA, E-cadherin, TGase 2, HSP-70, vWF, and VEGF. MAIN OUTCOME MEASURES: In the fissured tissue the sebaceous glands were strongly positive for PCNA and grew into the underlying fibromuscular tissue (24/42). Some hyperplastic sebaceous glands of prenatal cleft lip produced infundibular follicular cyst (9/17). The skin and mucosal epithelia from the postnatal cleft lip and palate (10/25) showed severe basal hyperplasia (11/25) and melanocyte infiltration (7/25). RESULTS: The immunostaining of MMP-3 and HSP-70 were strongly positive in the hyperplastic sebaceous glands and nearby atrophying muscle bundles of the fissured tissue, while MMP-9, MMP-10, and cathepsin G were almost negative. The immunoreactions of the other antibodies used in this study were similar between in the fissured tissues and in the normal controls. CONCLUSIONS: These data suggest that the over-expression of MMP-3 is closely related to the sebaceous gland hyperplasia, epithelial dysplasia, and the muscle degeneration, and that the over-expression of MMP-3 in the fissured tissue may continuously aggravate the cleft condition in the later life.
Adult ; Antibodies ; Cadherins ; Cathepsin G ; Cleft Lip* ; Follicular Cyst ; Humans ; Hyperplasia ; Lip ; Melanocytes ; Mouth Mucosa ; Outcome Assessment (Health Care) ; Palate* ; Proliferating Cell Nuclear Antigen ; Sebaceous Glands ; Skin ; Vascular Endothelial Growth Factor A

No abstract available.
Lymphoma* ; Thyroid Gland* ; Thyroiditis*

OBJECTIVE: To correlate existing evaluation tools with clinical information on Duchenne muscular dystrophy (DMD) patients following age and to investigate genetic mutation and its relationship with clinical function. METHOD: The medical records of 121 children with DMD who had visited the pediatric rehabilitation clinic from 2006 to 2009 were reviewed. The mean patient age was 9.9+/-3.4 years and all subjects were male. Collected data included Brooke scale, Vignos scale, bilateral shoulder abductor and knee extensor muscles power, passive range of motion (PROM) of ankle dorsi-flexion, angle of scoliosis, peak cough flow (PCF), fractional shortening (FS), genetic abnormalities, and use of steroid. RESULTS: The Brooke and Vignos scales were linearly increased with age (Brooke (y1), Vignos (y2), age (x), y1=0.345x-1.221, RBrooke2=0.435, y2=0.813x-3.079, RVignos2=0.558, p<0.001). In relation to the PROM of ankle dorsi-flexion, there was a linear decrease in both ankles (right and left R2=0.364, 0.372, p<0.001). Muscle power, Cobb angle, PCF, and FS showed diversity in their degrees, irrespective of age. The genetic test for dystrophin identified exon deletions in 58.0% (69/119), duplications in 9.2% (11/119), and no deletions or duplications in 32.8% (39/119). Statistically, the genetic abnormalities and use of steroid were not definitely associated with functional scale. CONCLUSION: The Brooke scale, Vignos scale and PROM of ankle dorsi-flexion were partially available to assess DMD patients. However, this study demonstrates the limitations of preexisting scales and clinical parameters incomprehensively reflecting functional changes of DMD patients.
Animals ; Ankle ; Child ; Cough ; Dystrophin ; Exons ; Gene Deletion ; Humans ; Knee ; Male ; Medical Records ; Muscles ; Muscular Dystrophy, Duchenne ; Range of Motion, Articular ; Scoliosis ; Shoulder ; Weights and Measures

The nephrotic syndrome in association with extrarenal malignancy is not an uncommon event. The membranous nephropathy is most frequently associated with various carcinomas of the lung, breast, stomach and colon. Though the exact causal relationship has not been determined completely, deposition of the immune complexes composed of antitumor antibody and tumor antigens in the subepithelium is most favorably accepted. We experienced a patient with previously diagnosed membranous nephropathy and subsequently demonstrated early gastric cancer during patient follow-up. After surgical resection proteinuria improved significantly. All physicians are strongly recommended to examine thoroughly and search carefully for possibility of concomitant occult malignancy when an aged patient, especially over 40 years old, is diagnosed as a nephrotic syndrome.
Adult ; Antigen-Antibody Complex ; Antigens, Neoplasm ; Breast ; Colon ; Follow-Up Studies ; Glomerulonephritis, Membranous* ; Humans ; Lung ; Nephrotic Syndrome ; Proteinuria ; Stomach ; Stomach Neoplasms*

The upstream stimulatory factor 1 (USF1) gene has been shown to play an essential role as the cause of familial combined hyperlipidemia, and there are several association studies on the relationship between USF1 and metabolic disorders. In this study, we analyzed two single nucleotide polymorphisms in USF1 rs2073653 (306A>G) and rs2516840 (1748C>T) between the case (dyslipidemia or obesity) group and the control group in premenopausal females, postmenopausal females, and males among 275 Korean subjects. We observed a statistically significant difference in the GC haplotype between body mass index (BMI) > or =25 kg/m(2) and BMI <25 kg/m(2) groups in premenopausal females ( chi-square=4.23, p=0.04). It seems that the USF1 GC haplotype is associated with BMI in premenopausal Korean females.
Adult ; Aged ; *Body Mass Index ; Cholesterol, HDL/blood ; Female ; Genotype ; *Haplotypes ; Humans ; Linkage Disequilibrium ; Male ; Middle Aged ; *Polymorphism, Single Nucleotide ; Premenopause ; Upstream Stimulatory Factors/*genetics