• Journal of Gastric Cancer
• /
• 제7권2호
• /
• pp.102-106
• /
• 2007

위에 발생하는 유암종(carcinoid tumor)은 위저부에 있는 장크롬친화 유사 세포(enterochromaffine-like cell)의 증식에 의해 발생하는 종양이다. 위유암종은 모든 위 신생물의 2% 이내로 드문 질환이나 최근 발생률이 증가하고 있다고 한다. 저자들은 다발성 용종의 형태로 발현된 위유암종을 1예 경험한 바 있어 이를 보고하는 바이다. 29세 여자가 3년 전 실신을 주소로 외부병원을 방문하여 시행한 혈액검사 상 혈색소 6.0 g/dl로 측정되었다. 위내시경 상 출혈을 동반한 용종성 병변이 관찰되었고, 내시경적 결찰술로 지혈하였다. 당시 시행한 병리조직 검사 상 유암종으로 진단되었다. 추적 관찰 중 용종성 병변의 출혈로 인한 철결핍성 빈혈이 계속되어 본원으로 전원되었다. 위내시경 상 중체부에서 분문부에 걸쳐 20개 이상의 크기가 다양한 용종성 병변들이 관찰되었다. 혈색소 수치는 9.0 g/dl이었다. 출혈을 동반한 다발성 용종성 위유암종 진단 하에 위전절제술을 시행하였다. 조직검사 결과 위유암종으로 진단되었고 림프절 전이는 없었다. 수술 18개월 후 혈색소 12.8 g/dl로 측정되었고 복부 초음파 상 재발 소견은 없었다. 본 증례와 같이 위에 다발성으로 발생한 용종 형태의 유암종이 지속적인 출혈을 동반하여 만성적인 빈혈을 유발하는 경우 적극적인 수술적 치료를 고려해야 한다.

• 한국동물위생학회지
• /
• 제38권3호
• /
• pp.199-203
• /
• 2015

An 8-year old intact female poodle was presented to clinics due to abdominal distension, anorexia, and labored breath associated with pleural effusion. Intra-operative findings revealed multiple neoplasm of the greater omentum, involving anterolateral abdominal wall, sterna surface in the pleural cavity and diaphragm. These masses were 0.1~0.5 cm in diameter and extended to ovaries, pancreas, and serosal surface of stomach. Microscopically, most neoplastic cells had oval nuclei with prominent nucleoli and abundant eosinophilic cytoplasm. In deeper area, neoplastic acinus or glandular structures showed invaginated growth resembling adenocarcinoma. High mitotic figures were observed. By immunohistochemistry, the neoplastic cells were strong positive both cytokeratin and vimentin. The present case described for malignant mesothelioma in a dog. Our findings might be helpful for diagnosis and information and helped the clinics choose the treatment including chemotherapy such as cisplatin.

• Tuberculosis and Respiratory Diseases
• /
• 제61권3호
• /
• pp.279-284
• /
• 2006

다발성 원발성 악성종양은 최근 발생 빈도가 증가하고 있으며 이는 암의 진단 방법의 개선 및 인구의 고령화, 유해물질에 대한 노출증가에 기인한다. 국내에서도 다발성 원발성 악성종양에 대한 연구가 진행되어왔으며, 김등, 윤등이 보고하였다. 그러나 삼중복암의 발생하는 빈도는 매우 낮은 것으로 보고되어있다. 저자들은 이화여대 동대문 병원 내과에 입원한 다발성 원발성 위암, 후두암, 폐암 환자의 1예를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

• Journal of the Korean Association of Oral and Maxillofacial Surgeons
• /
• 제36권6호
• /
• pp.543-547
• /
• 2010

Plasmacytoma is a rare malignant neoplasm in the head and neck region and comprises approximately 3% of all plasma cell tumors. This lesion is a unifocal, monoclonal, neoplastic proliferation of plasma cells that usually arises within the bone. Infrequently, it is observed in soft tissue, in which case, the term extramedullary plasmacytoma is used. Approximately 80-90% of extramedullary plasmacytomas involve the mucos-Associated-Lymphoid Tissue of the upper airways with 75% of these involving the nasal and paranasal regions. The plasmacytoma is usually detected in adult males, with an average age at diagnosis of 55 years. The male-to-female ratio is 3:1.Radiographically, the lesion may be seen as a well-defined, unilocularradioluceny with no evidence of a sclerotic border. Some investigators believe that this lesion represents the least aggressive part of the spectrum of plasma cell neoplasms that extend to multiple myeloma.Therefore, plasma cytoma is believed to have clinical importance. We report a case of extramedullary plasmacytoma in the right maxillary sinus of a 59-year-old male with review of the relevant literature.

• Journal of Chest Surgery
• /
• 제42권2호
• /
• pp.268-271
• /
• 2009

고립성 골형질세포종은 형질세포종양의 $3{\sim}5%$를 차지하는 드문 질환이며 특히, 늑골에 발생한 고립성 골형질세포종에 관해 국내에서는 아직 보고된 바가 없다. 54세 남자 한자가 검진 시 시행한 단순가슴 사진에서 폐종양으로 의심되는 병변이 있어 타병원에서 전원되었다. 전산화 단층 촬영 및 양전자 방출 단층 촬영 결과 좌측 6번째 늑골의 종양으로 진단되어 수술적 절제를 하였다. 병리 검사 결과 골형질세포종으로 진단되었으며 술 후 선별검사에서 다발성 골수종의 증거는 없었다. 술 후 방사선 치료는 하지 않았으며 2년째 추적 관찰 중이나 새로운 병변은 발견되지 않았다.

• Clinical and Experimental Pediatrics
• /
• 제58권2호
• /
• pp.69-72
• /
• 2015

Insulinoma, which arises from insulin-producing pancreatic beta cells, is a rare tumor in children. Only 5%-10% of insulinomas are malignant and undergo metastasis. We report a case of an 11-year-old girl who experienced hypoglycemia-related seizures induced by an insulinoma; after resection of the primary tumor, she developed hepatic focal nodular hyperplasia (FNH). Laboratory test results indicated marked hypoglycemia with hyperinsulinemia. Abdominal ultrasonography (US) and computed tomography results were normal; however, magnetic resonance imaging (MRI) showed a solid mass in the pancreatic tail. Therefore, laparoscopic distal pancreatectomy was performed. Two months after the surgery, an abdominal MRI revealed multiple nodular lesions in the liver. An US-guided liver biopsy was then performed, and histological examination revealed FNH without necrosis or mitotic activity. The patient has been free of hypoglycemia for 2 years, and recent MRI studies showed a decrease in the size of FNH lesions, without any evidence of metastasis. Even though no metastatic lesions are noted on imaging, close observation and follow-up imaging studies are required in a child with insulinoma that has malignant potential on histopathologic findings.

• Journal of Korean Neurosurgical Society
• /
• 제42권6호
• /
• pp.436-440
• /
• 2007

Objective : Spinal cord hemangioblastoma is an uncommon vascular neoplasm with a benign nature and is associated with von Hippel-Lindau (VHL) disease in 20-30% of patients. Total removal of these tumors without significant neurological deficit remains a great challenge. The purpose of this study was to investigate the efficacy of VHL mutation analysis and to evaluate surgical outcome of patients with spinal cord hemangioblastomas. Methods : This study included nine patients treated for spinal cord hemangioblastomas at our institute between December 1994 and March 2006. There were four male and five female patients. Mean age was 37.8 years. The mean follow-up period was 22.4 months. Magnetic resonance imaging (MRI) of the complete neuraxis was done in all cases and VHL mutation analysis was performed in three cases for a definite diagnosis. Results : Six patients had intramedullary tumor, and the remaining patients had intradural extramedullary lesions. Five patients were associated with VHL disease. The von Hippel-Lindau mutation analysis was done in three patients and two of them showed VHL gene abnormality. Tumors were located in the cervical cord in five cases and in the thoracic cord in four cases. All patients underwent surgical intervention, and total removal was achieved in six cases. All patients showed improvement or, at least, clinically stationary state. Surgical complications did not develop in any cases. Conclusion : Spinal hemangioblastoma in this series has been safely and effectively removed via a posterior approach. Postoperatively, clinical outcome was excellent in the majority of cases. The VHL mutation analysis was useful in patients with family history and in those with multiple hemangioblastomas.

• Journal of Korean Neurosurgical Society
• /
• 제29권1호
• /
• pp.15-22
• /
• 2000

Objective : This study was undertaken to evaluate the benefits and risks of the stereotactic biopsy in brain lesions. We assessed the diagnostic accuracy and morbidity rate associated with the stereotactic biopsy. Methods : The authors present a review of 47 patients, who underwent stereotactic biopsy using Cosman-Roberts-Wells(CRW) stereotactic apparatus during last six years. Results : Target locations were supratentorial in 36 cases, infratentorial in 9 and multiple in 2. According to pathological diagnosis, the largest group was neoplasm(29) followed by infection(9), infarction(2), cyst(2), and non-specific(5). Definitive diagnosis could be made in 42 of 47 cases(89.4%). When the mass lesion had been suspected as neoplastic condition, the diagnostic rate was 96.7%(29/30). It was being much higher than that of non-neoplastic lesion, 76.5%(13/17). The treatment modality was changed in 15 cases(32%) because the result of stereotactic biopsy was different from clinical diagnosis. Subsequent craniotomy after stereotactic biopsy was then performed in 6 cases, and the pathological diagnoses were precisely coincident in all of these cases. There were two complications(4.3%) : One intratumoral hemorrhage in glioblastoma and a transient hemiparesis in benign astrocytoma. There was no mortality in this series. Conclusion : The precise histological verification is crucial to determine the adequate treatment modality in intracranial lesions. Stereotactic biopsy is a safe and accurate diagnostic procedure for intracranial lesions with a low complication rate.

• Journal of Chest Surgery
• /
• 제30권7호
• /
• pp.729-732
• /
• 1997

흉벽에 발생한 악성 말초신경초종은 미국에서 Mark등a(1991)이 17례를 보고하였으나 한국에서는 아직까 지 발표된 예가 없다. 악성 말초신경초종은 악성 연부 육종의 10%에서 발생되며 대개 20세에서 50세 사이에 발생한다. 악성 말 초신경초종은 주로 좌골신경, 상완신경총, 천추총과 연관되어 발생하며, 가장 흔한 발생위치는 상지와 하지 의 근위부, 체간 등이며 드물게는 두경부에도 발생한다. 악성 연부조직 육종의 치료는 저급육종(low grade sarcoma)의 경우는 종양의 절제만으로 치유 가능하나 고급육종(high grade sarcoma)의 경우는 광범위 절제가 요구된다. 저자의 경우에는 50세 남자에서 다발성 거대종괴가 좌측 흉벽에 광범위하게 있었으며 병리소견상 저급 악 성 말초신경초종으로 판명되었다. 종괴들을 절제한후 발생한 흉벽결손은 15$\times$8 cm정도 였으며 Teflon을 이용하여 재건하였다. 수술후 환자 는 큰 문제 얼이 회복되었다.

• Journal of Chest Surgery
• /
• 제29권3호
• /
• pp.346-349
• /
• 1996

This 32 year old female patient underwent left radical mastectomy due to ductal carcinoma on May 1990, and treated with FAM (5-fluorouracil, Adriamycin and Mitomycin C) regimen postoperatively. However, right cervical Iymph node enlargement and facial edema progressively developed since December 199). On April 1994, operation was performed, and findings were as followes; x4$\times$5$\times$7 to 1 : 1 $\times$ 1 cm sized multiple enlarged and hyperemic Iymph nodes were scatterred throughout submandibular area to the junction of superior vents cave and pericardium, and partially invaded both anterior segmental lobe, sternum and both distal tip of clavicles. After radical dissection of the nodes of neck and mediastinal nodes, and wedge resection of both anterior segments of lung, and partial resection of both clavicle tips and total sternum. The both innominate veins and superior vena cava were partially obstructed by invaded cancer SVC reconstruction was done with preclotted 10$\times$ 10$\times$ 18mm Y shap d woven Dacron graft, which was anastomosed to the point of the junction of subclavian vein and jugular vein after cross clamping both veins and 2cm above the pericardial junction with one arm clamp. After maintaining blood drainage to the SVC from the right side, left innominate vein was anastomosed with 4-0 Prolene continuous running suture. Bone cement was used for resected sternal portion and clavicular ends were fixed to postal portion with 18 Gauge wires. The patient was treated with radiation and chemotherapy after discharge, and there were no evidence of regrowing of the mass nor obstruction of the graft inspite of no antithrombotic therapy.