• Investigative Magnetic Resonance Imaging
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• 제17권4호
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• pp.326-333
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• 2013

$H^1$ 자기공명분광술에서 악성 종양은 양성 병변보다 더 높은 농도의 대사물질들을 보여준다. 락테이트의 이중 첨단점은 악성 종양과 자궁내막증에서 나타났으며, 자궁내막증에서 더 높은 농도를 보였다. 자궁관난소농양과 난관염은 분명한 첨단점이 보이지 않는다. 유피낭종은 높은 수준의 지질 첨단점이 나타난다. 부난관 낭종 및 난포낭도 지질 첨단점을 보일 수 있지만, 지질의 농도는 유피낭종보다 현저히 낮다. $H^1$ 자기공명분광술은 낭성 난소병변의 대사 물 성분에 대한 유용한 정보를 제공할 수 있다.

• Clinical and Experimental Pediatrics
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• 제54권6호
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• pp.260-266
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• 2011

Purpose: Infantile hepatic hemangioendothelioma (IHHE) is the most common type of hepatic vascular tumor in infancy. We conducted this study to review our clinical experience of patients with IHHE and to suggest management strategies. Methods: We retrospectively analyzed the medical records of 23 IHHE patients (10 males, 13 females) treated at the Asan Medical Center between 1996 and 2009. Results: Median age at diagnosis was 38 days (range, 1 to 381 days). Seven patients (30%) were diagnosed with IHHE based on sonographically detected fetal liver masses, 5 (22%) were diagnosed incidentally in the absence of symptoms, 5 (22%) had congestive heart failure, 3 (13%) had skin hemangiomas, 2 (9%) had abnormal liver function tests, and 1 (4%) had hepatomegaly. All diagnoses were based on imaging results, and were confirmed in three patients by histopathology analysis. Six patients were observed without receiving any treatment, whereas 12 received corticosteroids and/or interferonalpha. One patient with congestive heart failure and a resectable unilobar tumor underwent surgical resection. Three patients with congestive heart failure and unresectable tumors were managed by hepatic artery embolization with/without medical treatment. At a median follow-up of 29 months (range, 1 to 156 months), 21 (91%) patients showed complete tumor disappearance or >50% decrease in tumor size. One patient died due to tumor-related causes. Conclusion: IHHE generally has a benign clinical course with low morbidity and mortality rates. Clinical course and treatment outcome did not differ significantly between medically treated and non-treated groups. Surgically unresectable patients with significant symptoms may be treated medically or with hepatic artery embolization.

• Clinical and Experimental Pediatrics
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• 제51권12호
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• pp.1363-1367
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• 2008

해면 혈관종은 비교적 양성의 병변이며 다량의 뇌출혈을 일으키는 것은 드물어서 수술의 적응증에 대해 논란의 여지가 있다. 그러나 특히 소뇌 같은 후두와나 뇌간에서 발생한 해면 혈관종에서의 출혈은 제한된 공간으로 인해 비가역적인 뇌손상을 일으킬 수 있으며 이로 인해 사망한 경우도 보고되고 있어서 소뇌의 압박증상이 있으면 응급수술을 해야 한다. 병변으로부터 반복되는 출혈로 인해 뒷목 근육통으로 오인되었던, 소아에서는 드물게 소뇌에 생긴 해면 혈관종 1예를 보고하는 바이다.

• Archives of Plastic Surgery
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• 제36권4호
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• pp.497-499
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• 2009

Purpose: Leiomyoma is a rare benign tumor of nonstriated muscles. Leiomyoma is most commonly found in the uterus and rarely occur in the hand. 150 cases of leiomyoma of the hand have been reported in the English literature; however, to the best of our knowledge only four of these have been in children and none were reported in Korean literature. We present a case of leiomyoma in the hand of a 8 - year - old boy, which is a rare site for localization and unusual for age. Methods: A 8 - year - old boy presented with a painless mass on the ulnar side of his thumb. Physical examination revealed a $1.2{\times}1.2cm$ round, rubbery mass that was nontender to palpation. The vascular, sensory, and motor exams were otherwise unremarkable. Further evaluation with CT demonstrated an enhancing mass at dorsoulnar aspect of 1st proximal phalangeal region suggestive of a hemangioma versus other enhancing solid mass. The diagnosis of a leiomyoma was confirmed following surgical excision with histologic evaluation. Results: At 3 months follow - up, the incision was healed, motor and sensory function were intact, and there were full range of motion. Neither recurrence nor postoperative complication were observed. Conclusion: Leiomyoma is a rare tumor of the hand, especially in children. Diagnosing hand tumors in children is more difficult than in adults, hand surgeons should be aware of the diagnostic possibilities based on examination and imaging of a hand tumor ; however, surgical excision with histologic examination is required for definitive diagnosis.

• 한국방사선학회논문지
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• 제8권1호
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• pp.27-33
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• 2014

건강에 대한 관심의 증대로 의료영상이 빠르게 증가하고 있으며, 컴퓨터 기술의 발전으로 의료영상의 디지털화가 빠르게 진전되어 PACS가 의료현장에 도입되었다. 이러한 현상에 의한 의료영상 생산의 증가는 의료영상을 판독하여야 하는 영상의학과 전문의의 업무량을 증가하게 하였다. 이러한 추세에 따라 컴퓨터를 이용한 보조 진단의 필요성이 대두되어 의료영상 판독 분야에 CAD라는 용어가 생겨나게 되었다. 본 연구에서는 디지털 X-선 유방촬영장치에 의하여 획득된 영상의 판독을 위한 CAD 알고리즘을 제안하였다. 제안된 알고리즘을 Visual C++로 프로그램하여 실험하였다. 본 연구에 사용한 일곱 샘플영상을 CAD 알고리즘으로 실행한 결과 다섯 샘플의 결과는 양성종양 및 유방암으로 확인되었고 두 샘플 영상은 error처리 되었다. 본 연구에서 제시한 알고리즘과 이를 구현한 프로그램을 이용한다면 판독업무에 많은 도움이 될 것이며, 유방암의 조기발견에 크게 기여할 것으로 사료된다.

• Journal of Chest Surgery
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• 제30권1호
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• pp.116-118
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• 1997

기관지내 지방종은 주로 기관지 근위부에서 발병하면서, 그 원위부의 폐실질에 비가역적 손상을 입히는 아주 드문 질환이다. 이는 조직학적으로는 양성종양이다. 그러나 진단 및 치료가 늦을 경우에는 비가역적 폐실질 손상 및 기관지확장증 등을 유발시킬 수 있다. 가능하다면 가장 좋은 치료방법은 기관지 내시경을 이용한 종양 제거술이다. 그러나 내시 경을 이용하여 종양 제거가 불가능하거나, 진단이 불명확한 경우에는 폐엽절제술 또는 전폐적출술 등을 포함한 개흉술이 필요한 경우가 많은데, 이는 이들 대부분이 폭넓은 폐실질 손상을 동반하고 있기 때문이다. 우리는 기관지 내경을 완전히 막으면서. 그 원위부에 비가역적 손상을 일으킨 기관지내 지방종 1례를 경험하였기에 이를 일반적인 기관지내 지방종의 임상증상, 진단 방법, 그리고 치료방법 등과 함께 보고하는 바이다.

• Journal of Chest Surgery
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• 제37권1호
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• pp.102-104
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• 2004

염증성 근섬유 아세포종은 주로 어린이와 젊은 성인에서 발생하는 고형 종양으로, 고립성 폐 결절의 약 0.7%를 차지한다. 1937년 처음으로 폐에서 발생한 예가 보고된 이후 장간막(mesentery)이나 심장 식도 부위(cardioesophageal region)에 발생한 것들이 보고되고 있다. 이것은 조직학적으로는 양성이지만 국소 침습성과 재발성 때문에 악성을 완전히 배제하기 어렵다. 최근 본 병원에서 좌측 폐에 발생한 염증성 근섬유 아세포종을 수술적 절제후 재발 소견 없이 추적 관찰 중이다.

• 대한핵의학회지
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• 제35권4호
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• pp.274-279
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• 2001

A large superior mediastinal mass was found incidentally by ultrasonography in a 60-year-old man. There was an abnormal accumulation of Tl-201 in the lower pole of left thyroid gland, extending into left superior mediastinum on Tc-99m pertechnetate/Tl-201 subtraction scan. Laboratory findings relating thyroid and parathyroid were all within normal range. We considered the mass as a non-functioning parathyroid adenoma tentatively. However, subsequent surgery and pathologic examination revealed the mass to be a benign mixed thymoma. We report a case of patient with thymoma showing unusual Tc-99m pertechnetate/Tl-201 subtraction imaging and laboratory findings, and suggest to consider the possibility of other mediastinal tumors rather than parathyroid adenoma.

• Molecules and Cells
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• 제39권12호
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• pp.877-887
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• 2016

Tazarotene-induced gene 1 (TIG1) is a retinoic acid-inducible protein that is considered a putative tumor suppressor. The expression of TIG1 is decreased in malignant prostate carcinoma or poorly differentiated colorectal adenocarcinoma, but TIG1 is present in benign or well-differentiated tumors. Ectopic TIG1 expression led to suppression of growth in cancer cells. However, the function of TIG1 in cell differentiation is still unknown. Using a yeast two-hybrid system, we found that transmembrane protein 192 (TMEM192) interacted with TIG1. We also found that both TIG1A and TIG1B isoforms interacted and co-localized with TMEM192 in HtTA cervical cancer cells. The expression of TIG1 induced the expression of autophagy-related proteins, including Beclin-1 and LC-3B. The silencing of TMEM192 reduced the TIG1-mediated upregulation of autophagic activity. Furthermore, silencing of either TIG1 or TMEM192 led to alleviation of the upregulation of autophagy induced by all-trans retinoic acid. Our results demonstrate that the expression of TIG1 leads to cell autophagy through TMEM192. Our study also suggests that TIG1 and TMEM192 play an important role in the all-trans retinoic acid-mediated upregulation of autophagic activity.

• Journal of Genetic Medicine
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• 제13권1호
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• pp.36-40
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• 2016

Tuberous sclerosis complex (TSC, MIM#191100) is an autosomal dominant neurocutaneous syndrome caused by mutation or deletion of TSC1 encoding hamartin or TSC2 encoding tuberin and characterized by seizure, mental retardation, and multiple hamartomas or benign tumors in the skin, brain, retina, heart, kidney, and lungs. The TSC2 gene on chromosome 16p13.3 lies adjacent to the PKD1 gene which is responsible for autosomal dominant polycystic kidney disease (MIM#173900). The TSC2/PKD1 contiguous gene syndrome (TSC2/PKD1 CGDS, MIM#600273) is caused by deletion of both TSC2 and PKD1 gene. We recently experienced a 15 month-old boy and a 26 month-old girl with TSC2/PKD1 CGDS confirmed by multiplex ligation-dependent probe amplification (MLPA) analysis. They showed not only typical neurologic manifestations of TSC such as epilepsy, subependymal nodules, and subcortical tubers, but also polycystic kidney disease. The contiguous gene syndrome involving PKD1 and TSC2 should be suspected in children with enlarged polycystic kidneys and TSC. MLPA analysis is a useful method for the genetic confirmation of TSC2/PKD1 CGDS.