Tuberculoma, once the most frequent cause of intracranial mass lesion, are now rare. Except in cases in which meningitis develops owing to extension to the subarachnoid space, the symptoms of them are those of an expanding cerebral or cerebellar mass. A 18 years old female was admitted to Chungnam National University Hospital complaining of headache and severe vomiting. Neurological examination showed severe papilledema, trunkal ataxia and mild ataxic gait. Chest P-A and skull X-rays showed non specific finding. Total removal of mass in right cerebellar hemisphere after exploration of posterior fossa was done and it was confirmed of tuberculoma histologically. Postoperative course was uneventful and discharged with good health.
Adolescent ; Ataxia ; Chungcheongnam-do ; Female ; Gait ; Headache ; Humans ; Meningitis ; Neurologic Examination ; Papilledema ; Skull ; Subarachnoid Space ; Thorax ; Tuberculoma* ; Vomiting

Tuberculoma, once the most frequent cause of intracranial mass lesion, are now rare. Except in cases in which meningitis develops owing to extension to the subarachnoid space, the symptoms of them are those of an expanding cerebral or cerebellar mass. A 18 years old female was admitted to Chungnam National University Hospital complaining of headache and severe vomiting. Neurological examination showed severe papilledema, trunkal ataxia and mild ataxic gait. Chest P-A and skull X-rays showed non specific finding. Total removal of mass in right cerebellar hemisphere after exploration of posterior fossa was done and it was confirmed of tuberculoma histologically. Postoperative course was uneventful and discharged with good health.
Adolescent ; Ataxia ; Chungcheongnam-do ; Female ; Gait ; Headache ; Humans ; Meningitis ; Neurologic Examination ; Papilledema ; Skull ; Subarachnoid Space ; Thorax ; Tuberculoma* ; Vomiting

Primary rhabdomyosarcoma of the frontal and temporal bone is very rare. Rhabdomyosarcoma is usually a relentless, progressive which results in death of patients in a relatively short time. The authors report a case of rhabdomyosarcoma arisen right frontotemporal bone and reviewed the literatures.
Humans ; Rhabdomyosarcoma* ; Temporal Bone

Congenital intradural intramedullary ependymal cysts of the spinal canal are very rare. The following case history is presented to emphasize the clinical features and to lead to a discussion of the origin of these cysts. We report our case with the brief review of the articles.
Spinal Canal

Encephalocraniocutaneous lipomatosis (ECCL) is a rare congenital neurocutaneous syndrome that was characterized by unilateral, smooth, hairless fatty tissue nevi of the scalp, termed nevus psiloliparus, facial lesions, multiple anomalies involving the eye, and ipsilateral porencephalic cysts with cortical atrophy, cranial asymmetry, marked developmental delays, and mental retardation. A 12-month-old boy was referred to our clinic for evaluation of non-scarring alopecia on the left side with an underlying fatty mass in the left parietal scalp and left-sided multiple periocular masses. It showed a large lipomatous mass on the scalp with overlying alopecia. Multiple skin tags and defects in the left periocular area were also observed. Additional ocular anomalies included epibulbar lipodermoid, iris coloboma, and localized peripapillary hypopigmentation lesions. After complete excision, the wound was covered with a local flap. The histologic examination revealed a mass surrounded by a well-developed capsule within the dermal layer, adipose tissue and connective tissue septa extending into the reticular dermis. No recurrence was observed at follow-up. It is essential to differentiate suspected ECCL from other syndromes which present with epibulbar chorisotomas. Neuroimaging, and pathological studies may be helpful for correct diagnosis. We will correct multiple periocular lesions in preschool age and follow up developmental problems like developmental delay and mental retardation constantly.
Adipose Tissue ; Alopecia ; Atrophy ; Coloboma ; Connective Tissue ; Dermis ; Eye ; Eye Diseases ; Follow-Up Studies ; Humans ; Hypopigmentation ; Infant ; Intellectual Disability ; Iris ; Lipomatosis ; Neurocutaneous Syndromes ; Neuroimaging ; Nevus ; Recurrence ; Scalp ; Skin

Wegener's granulomatosis (WG) is a systemic disease characterized by necrotizing granulomas and vasculitis involving the upper and lower respiratory tract as well as the kidneys. Limited form of WG usually involves the head and neck, lacks renal involvement, and may not progress to generalized disease. We report the case of limited form of WG who presented not systemic symptom but several times relapsed multiple ulcerating lesions on the face, uveitis and keratoconjunctivitis. A 23 year-old female initially presented with ulcerative skin lesions on the left cheek and nose. The skin lesion had commenced as an ulcerative and nodulopapular lesion on her right cheek initially, 8 months ago. Subsequently, there was progression of the disease to her left cheek and nose. The patient was treated with oral prednisolone and oral cyclophosphamide. Two weeks later, skin lesion had started to heal, oral prednisolone tapered to 15 mg. Eight weeks later, all of skin lesions were healed well. With silicone gel sheets and Laser therapies, we gained excellent cosmetic results. In the aesthetic aspect, early recognition of rare variants of limited form of WG, facial chronic ulcerative wounds that are nonresponsive to conservative treatment, is very important as appropriate therapy can prevent facial mutilation.
Cheek ; Cosmetics ; Cyclophosphamide ; Female ; Granuloma ; Head ; Humans ; Keratoconjunctivitis ; Kidney ; Laser Therapy ; Neck ; Nose ; Prednisolone ; Respiratory System ; Silicone Gels ; Skin ; Ulcer ; Uveitis ; Vasculitis ; Wegener Granulomatosis

Oligodendrolioma constitutes 3-12% of intracranial gliomas and is a slowly growing, benign tumor. Though uncommon in childhood and adolescenee, most tumors are idertified in the adult with peak at the age of 40 years. It has a predilection for frontal lobe and shows characteristic microscopic findings. Calcareous deposits arre demonstrated radiologically in 40-60%. The authors have experienced a case of large oligodendroglioma arising from the right parietal lobe in child and reviewed the literatures.
Adult ; Child* ; Frontal Lobe ; Glioma ; Humans ; Oligodendroglioma* ; Parietal Lobe

Intramedullary spinal teratoma is extremely rare, especially in the thoracic region. This case, which we have experienced recently, is reported with a review of literatures.
Teratoma*

No abstract available.
Behcet Syndrome* ; Renal Insufficiency*

OBJECTIVES: The aim of study was to examine the prevalence of night eating syndrome(NES) and its correlates in schizophrenic outpatients. METHODS: The 14 items of self-reported night eating questionnaire(NEQ) was administered to 201 schizophrenic patients in psychiatric outpatient clinic. We examined demographic and clinical characteristics, body mass index(BMI), subjective measures of mood, sleep, binge eating, and weight-related quality of life using Beck's Depression Inventory(BDI), Pittsburgh Sleep Quality Index(PSQI), Binge Eating Scale(BES) and Korean version of Obesity-Related Quality of Life Scale(KOQoL), respectively. RESULTS: The prevalence of night eaters in schizophrenic outpatients was 10.4%(21 of 201). Comparisons between NES group and non-NES group revealed no significant differences in sociodemographic characteristics, clinical status and BMI. Compared to non-NES, patients with NES reported significantly greater depressed mood and sleep disturbance, more binge eating pattern, and decreased weight-related quality of life. While 'morning anorexia' and 'delayed morning meal'(2 of 5 NES core components in NEQ) were not differed between groups, 'nocturnal ingestions', 'evening hyperphagia', and 'mood/sleep' were more impaired in NES group. CONCLUSION: These findings are the first to describe the prevalence and its correlates of night eaters in schizophrenic outpatients. These results suggest that NES has negative mental health implications, although it was not associated with obesity. Further study to generalize these results is required.
Ambulatory Care Facilities ; Bulimia ; Depression ; Eating* ; Humans ; Mental Health ; Obesity ; Outpatients* ; Prevalence* ; Quality of Life