• 수면정신생리
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• 제3권1호
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• pp.68-78
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• 1996

연구목적 : 각종 질병에서 임상적으로 인지기능평가 및 선별검사로 유용하게 사용되고 있는 정신상태소검사(MMSE)와 간이인지평가척도(BCRS)가 비외상성 피질하 뇌혈관질환 환자에서 인지기능평가에 유용한가를 평가하기 위하여 본 연구를 시도하였다. 연구대상 및 방법 : 1995년 1월 1일부터 9월 30일까지 경희대 한방병원 및 고려대부속병원 신경과에 입원하거나 통원치료중인 비외상성 피질하 뇌혈관 질환 환자 85명과 정상대조군 195명을 대상으로 하였다. 또한 환자군중 65명을 뇌영상 촬영소견에 따라 좌반구손상(21명), 우반구손상(31명), 양반구손상(13명) 환자군으로 나누었다. 이들에게 인지기능은 벤튼신경심리검사(Benton Neuropsycho-logical Assessment : BNA)로, 일상생활기능면은 노인상태에 대한 보호자 측정척도(Geriatric Evaluation by Relative's Rating Instrument : GERRI) 및 도구적 일상생활 활동척도 (Instrumental Activities of Daily Living Scale : IADLs)를 이용하여 평가하였다. 연구결과 : 1) BNA는 좌우지남력과 운동지속성을 제외하고는 모든 하위항목에서 유의한 차이를 보였으나 MMSE 총점수와 하위척도 모두든 환자군과 정상대조군간에 유의한 차이를 보이지 않았다. BCRS는 최근기억과 자신돌봄항목에서만 두 군간에 유의한 차이를 보였다. 2) 편측성에 따른 세군간의 비교에서 BNA는 촉각형태검사(좌측), 손가락위치검사(좌, 우측)에서 세군간 유의한 차이를 보였으나 MMSE나 BCRS에서는 유의한 차이를 보이지 않았다. 3) 일상생활기능과 MMSE, BCRS와의 상관관계에서 정상대조군에서는 MMSE, BCRS의 총점수 및 하위 척도점수가 노인상태에 대한 보호자 측정척도(GERRI)의 인지기능 하위척도점수와만 유의한 상관관계를 갖는 반면, 환자군에서는 노인상태에 대한 보호자 측정척도(GERRI)의 인지기능척도점수 이외에도 사회적 기능척도점수 및 도구적 일상생활 활동척도(IADLs) 점수와도 유의한 상관을 가져 두 군간에 차이를 보였다. 결론 : MMSE와 BCRS는 비외상 피질하 뇌혈관질환 환자에서 인지기능평가나 편측성 구분에 유용하지 않았다. 그러나 이들 검사는 환자군에서 일상생활기능과 같은 기능수준을 반영하고 있음을 보여 주었다.

• Journal of Korean Neurosurgical Society
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• 제59권2호
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• pp.168-171
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• 2016

Choroidal fissure cysts are often incidentally discovered. They are usually asymptomatic. The authors report a case of growing and hemorrhagic choroidal fissure cyst which was treated surgically. A 22-year-old female presented with headache. Cranial MRI showed a left-sided choroidal fissure cyst. Follow-up MRI showed that the size of the cyst had increased gradually. Twenty months later, the patient was admitted to our emergency department with severe headache. MRI and CT showed an intracystic hematoma. Although such cysts usually have a benign course without symptoms and progression, they may rarely present with intracystic hemorrhage, enlargement of the cyst and increasing symptomatology.

• Archives of Plastic Surgery
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• 제45권2호
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• pp.171-176
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• 2018

Central venous stenosis is a rare cause of unilateral breast edema occurring in hemodialysis patients that needs to be differentiated from other differential diagnoses, including, but not limited to, inflammatory breast carcinoma, mastitis, lymphedema, and congestive heart failure. All reports of similar cases in the available literature have described improvement or resolution of the edema after treatment. Herein, we report and discuss the pathophysiology of breast edema formation in a patient who presented with massive left-sided breast edema 7 years after being diagnosed with central venous stenosis. Medical and minimally invasive therapy had not been successful, so she underwent reduction mammoplasty to relieve the symptoms.

• 대한수학회지
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• 제55권5호
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• pp.1193-1205
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• 2018

We focus our attention on a ring property that nilpotents are contained in the Jacobson radical. This property is satisfied by NI and left (right) quasi-duo rings. A ring is said to be NJ if it satisfies such property. We prove the following: (i) $K{\ddot{o}}the^{\prime}s$ conjecture holds if and only if the polynomial ring over an NI ring is NJ; (ii) If R is an NJ ring, then R is exchange if and only if it is clean; and (iii) A ring R is NJ if and only if so is every (one-sided) corner ring of R.

• 대한수의학회지
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• 제50권4호
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• pp.319-322
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• 2010

A 3-day-old Appaloosa colt was examined because of acute onset of ataxia, left-sided head tilt, fever and heart murmur. The foal continued to nurse but became increasingly depressed and mild colic. On plain radiological examination, the foal was normal. Uroperitoneum was diagnosed following abdominocentesis. Postmortem examination revealed bladder rupture. The lesion was in the dorsomedial part of the bladder wall. We suggested that the cause of bladder rupture was parturient trauma. Even though the rupture was associated with trauma, the margin of rupture of bladder was clearly smooth and regular.

• Journal of Chest Surgery
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• 제20권3호
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• pp.603-609
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• 1987

The clinical, investigative, and surgical experiences were reviewed in four patients with congenitally corrected transposition of the great arteries who presented to the National Medical Center between August 1983 and August 1985. This condition is very rare congenital anomaly defined as the combination of atrioventricular discordance and transposition of the great arteries. Examples of primitive [single] ventricle inverted [that is, left sided in situs solitus] with outflow chamber were excluded in this paper. According to the sequential arrangement of the hearts there were two cases of [S,L,L] and two cases of [I,D,D]. The surgical approach should be focused on minimizing the risk of heart block and increasing the degree of relief of pulmonary outflow tract obstruction [POTO]. We experienced complete heart block in two cases of [S,L,L] and significant residual POTO in one case of [S,L,L] and one case of [I,D,D] postoperatively. There were one hospital mortality caused by complete heart block and residual POTO and two delayed mortalities caused by congestive heart failure and sepsis respectively.

• The Korean Journal of Pain
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• 제18권2호
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• pp.232-234
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• 2005

Stellate ganglion block (SGB) is one of the most widely used treatment modalities for a broad range of disorders, including otolaryngologic indications such as Meniere's disease and sudden hearing loss. We present a case of a vertiginous attack following SGB for the management of Meniere's disease. A 31-year-old female, suffering from Meniere's disease, underwent repeated right side SGBs with 6 ml of 1% mepivacaine after negative aspiration tests for blood. The eleventh block was performed in the usual manner. Several seconds after injection, she showed agitation, anxiety, nystagmus, and left-sided tinnitus. Two minutes later, her tinnitus and nystagmus were resolved. Fifteen minutes after injection, she experienced acute onset of severe vertigo, nausea, and vomiting. However, her symptoms were gradually alleviated within two hours.

• Journal of Korean Neurosurgical Society
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• 제42권6호
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• pp.478-480
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• 2007

Unruptured non-traumatic dissecting aneurysm in the M4 segment of the middle cerebral artery (MCA) accompanied by complete occlusion of the ipsilateral internal cerebral artery (ICA) has never been reported. A 41-year-old man presented with an infarction manifesting as left-sided weakness and dysarthria. Magnetic resonance angiography revealed a subacute stage infarction in the right MCA territory and complete occlusion of the right ICA. Angiography demonstrated aneurysmal dilatation of the M4 segment of the right MCA. Surgery was performed to prevent hemorrhage from the aneurysm. The aneurysm was proximally clipped guided by Navigation-CT angiography and flow to the distal MCA was restored by superficial temporal artery-middle cerebral artery (STA-MCA) anastornosis. We report this rare case with literature review.

• 대한수의학회지
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• 제58권2호
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• pp.111-114
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• 2018

A 6-year-old female domestic short hair cat presented with acute onset of vomiting, anorexia, lethargy, and tachypnea. The cat was apparently healthy prior to presentation without history of trauma. On diagnostic imagings, the entire stomach and spleen were detected in the thoracic cavity. An emergent celiotomy was performed, and a type-4 hiatal hernia was confirmed; the stomach, spleen, pancreas, and duodenum were herniated through the esophageal hiatus. It was corrected using phrenicoplasty, esophagopexy, and left-sided gastropexy and there was no recurrence 16 months after surgery. This is the first case report of an idiopathic type-4 hiatal hernia in a cat.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
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• 제40권5호
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• pp.246-249
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• 2014

Eagle syndrome is a rare condition caused by elongation of the styloid process or calcification of the stylohyoid ligament. Patients with Eagle syndrome typically present with dysphagia, dysphonia, cough, voice changes, otalgia, sore throat, facial pain, foreign body sensation, headache, vertigo, and neck pain. Here we report a case in which the patient initially presented with sore throat, left-sided facial pain, and cough. This case report provides a brief review of the diagnosis and nonsurgical management of this rare syndrome.