• 제목/요약/키워드: patch mass

검색결과 68건 처리시간 0.028초

우심방에 발생한 원발성 악성 림프종의 수술적 치험 - 1예 보고 - (Primary Malignant Cardiac Lymphoma in Right Atrium - A case report-)

  • 최원석;한일용;전희재;이양행;황윤호;조광현
    • Journal of Chest Surgery
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    • 제41권3호
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    • pp.369-372
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    • 2008
  • 심장에 발생하는 원발성 악성 림프종은 매우 드물다. 68세 남자 환자가 점점 심해지는 호흡곤란으로 본원 흉부외과에 입원하였다. 심장 초음파, 흉부컴퓨터단층촬영 후, 우심방과 우심실에 걸쳐 있는 거대 종양을 발견하였다. 뇌경색 등의 위험과 혈역학적 불안정으로 응급수술을 결정하였다. 우측 심장에 있는 거대 종양을 심방 중격의 일부와 전외측 우심방 벽을 함께 포함하여 제거하고, 우형 심내막 패치로 재건하였다. 최종 조직검사상 원발성 악성 림프종으로 진단되었으며, 환자와 보호자가 경제적 이유 등으로 항암치료를 거부하고 귀가 퇴원을 하였다.

Multiple Large Cysts Arising from Nevus Comedonicus

  • Jeong, Hii-Sun;Lee, Hye-Kyung;Lee, Seung-Hyun;Kim, Hyoung-Suk;Yi, Sang-Yeop
    • Archives of Plastic Surgery
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    • 제39권1호
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    • pp.63-66
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    • 2012
  • Nevus comedonicus is a type of hamartoma that arises from a developmental anomaly of the mesodermal part of the pilosebaceous gland. In most cases of nevus comedonicus, an acne-like skin condition develops. Repeated inflammation can cause a morphological change to the cyst, papule, to abscess. We experienced a case of congenital nevus comedonicus, which led to the formation of large multiple cysts. A 50-year-old man was referred with a $12.5{\times}10cm$ lobulated mass on the posterior neck and upper back. The patient had a widespread presence of nevus comedonicus in the region ranging from the right superior chest to the posterior neck. The patient had a 30-year history of six prior excisions. A magnetic resonance imaging review led to a diagnosis of nevus comedonicus. Surgical treatment consisted of excision of the mass and wide excision for the patch type of nevus comedonicus around the neck. On histopathology, multiple masses were diagnosed as typical cysts containing keratinized tissue. The diffuse comedone lesions were diagnosed as nevus comedonicus. This case shows that large, multiple cysts can occur as a long-term complication of nevus comedonicus, and also highlights the importance of radical resection to prevent its further invagination.

A Sensitive, Efficient, and Cost-Effective Method to Determine Rotigotine in Rat Plasma Using Liquid-Liquid Extraction (LLE) and LC-MRM

  • Kim, Ji Seong;Jang, Yong Jin;Kim, Jin Hee;Kim, Jin Hwan;Seo, Jae Hee;Park, Il-Ho;Kang, Myung Joo;Choi, Yong Seok
    • Mass Spectrometry Letters
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    • 제13권4호
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    • pp.146-151
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    • 2022
  • Rotigotine (RTG) is a non-ergot dopamine agonist used to manage the early stage of Parkinson's disease (PD) as transdermal patch. However, the poor medication compliance of PD patients and skin issues related with repeated applications of RTG patches lead to the search for alternative formulations and it also requires appropriate analytical methods for their in vivo evaluation. Thus, here, a sensitive, efficient, and cost-effective method to determine RTG in rat plasma using liquid-liquid extraction (LLE) and multiple reaction monitoring was developed. The use of 20 µL of rat plasma for sample treatment, 8-OH-DPAT as the internal standard, and methyl tert-butyl ether as the LLE solvent in the present method gives it advantages over previous methods for the analysis of RTG in biological samples. The good analytical performance of the developed method was confirmed in specificity, linearity (the coefficient of determination ≥0.999 within 0.1-100 ng/mL), sensitivity (the lower limit of quantitation at 0.1 ng/mL), accuracy (81.00-115.05%), precision (≤10.75%), and recovery (81.00-104.48%) by following the FDA guidelines. Finally, the applicability test of the validated method to the in vivo evaluation of a RTG formulation showed that the present method is the only method which can be accurately applied to that longer than 24 hours, critical for the development of formulations with reduced dosing frequencies. Therefore, the present method could contribute to the development of new RTG formulations helpful to people suffering from PD.

Acute Subdural Hematoma after Accidental Dural Puncture During Epidural Anesthesia

  • Kim, Il-Sup;Lee, Sang-Won;Son, Byung-Chul;Hong, Jae-Taek
    • Journal of Korean Neurosurgical Society
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    • 제40권5호
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    • pp.384-386
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    • 2006
  • Acute subdural hematoma is an exceptionally rare, but life-threatening complication of spinal anesthesia. The authors report here on a case of acute subdural hematoma in a 52-year-old male who underwent an arthroscopic knee joint operation under spinal epidural anesthesia due to tearing of the medial meniscus. He complained of headache after surgery. Computed tomography[CT] revealed acute subdural hematoma in the right fronto-tempo-parietal area. The headache progressed in spite of analgesics and bed rest; two weeks later, the CT showed subacute subdural hematoma with a mass effect. The patient improved after surgical decompression. The pathogenesis of subdural hematoma formation after dural puncture is discussed and we briefly review the relevant literature. Prolonged and severe postdural puncture headache[PDPH] should be viewed with suspicion and investigated promptly to rule out any intracranial complications. Immediate treatment of the PDPH with an epidural blood patch to prevent further CSF leakage should be considered.

흉골에 발생한 연골육종: 수술 치험 1례 (Chondrosarcoma of the Sternum - One Case Report -)

  • 정진용
    • Journal of Chest Surgery
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    • 제24권8호
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    • pp.802-806
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    • 1991
  • Primary neoplasms of the ribs and sternum are rare. Most primary bony chest wall neoplasms are malignant, and chondrosarcoma is the most common malignancy in this location The etiology of chondrosarcoma is unknown. Definitive diagnosis of chondrosarcoma can only be made pathologically. The natural history of chest wall chondrosarcoma is one of slow growth and local recurrence. Most tumors of the sternum require wide resection and reconstruction procedures, with potentially serious postoperative problems. Advances in chest wall reconstruction primarily through refinement in muscle transposition and clarification of the functional anatomy and blood supply of trunk muscles, has resulted in a more aggressive resection of the these tumors . Recently we experienced a case with chondrosarcoma of the sternum. A 56 year-old man was admitted to our hospital due to painless, slowly enlarging mass at the left sternoclavicular junctional area. The chest radiograph strongly suggested an underlying cartilaginous neoplasm owing to the appearance of typical flocculent and curvilinear calcifications within the lesion. On CT of the chest, the tumor exhibited a scalloped or lobulated contour, hypodensity of the nonmineralized component in comparison to adjacent muscle, and characteristic stippled cartilaginous matrix mineralization, also typical for cartilaginous neoplasm. The patient underwent wide resection of the chest wall tumor include with a 2-3cm margin of normal tissue on all sides and the thoracic skeletal defect was reconstructed with polytetrafluoroethylene [Gore-Tex] soft-tissue patch. Soft tissue reconstructive procedure was done with the pectoralis major muscle transposition. The patient had an uneventful postoperative course and discharged without adjuvant treatment such as radiation and chemotherapy.

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폐흡충증 (Paragonimiasis)

  • 오제열;안철민;김태선;황의석;김형중;김성규;이원영
    • Tuberculosis and Respiratory Diseases
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    • 제39권1호
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    • pp.103-108
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    • 1992
  • Pulmonary paragonimiasis is the infectious disease of lung, due to 'Paragonimus westermani'. The clinical manifestations are various, and the main symptoms are chronic cough and persistent hemoptysis. Radiological findings mainly include thin walled cyst, migrating patch pulmonary infiltration, transient linear shadow, and hydropneumothorax, etc. The differential diagnosis should include pulmonary tuberculosis, pneumonia, other parasitic diseases, and rarely lung malignancy if the mass-like lesion is present. Recently, the incidence of paragonimiasis is very low. But the physicians should suspect paragonimus infection, if the patient has chronic respiratory symptom such as hemoptysis and lives in the endemic area such as Korea. A case of pulmonary paragonimiasis confirmed by histological basis of lung was presented with a review of the literature.

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Performance of a Planar Leaky-Wave Slit Antenna for Different Values of Substrate Thickness

  • Hussain, Niamat;Kedze, Kam Eucharist;Park, Ikmo
    • Journal of electromagnetic engineering and science
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    • 제17권4호
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    • pp.202-207
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    • 2017
  • This paper presents the performance of a planar, low-profile, and wide-gain-bandwidth leaky-wave slit antenna in different thickness values of high-permittivity gallium arsenide substrates at terahertz frequencies. The proposed antenna designs consisted of a periodic array of $5{\times}5$ metallic square patches and a planar feeding structure. The patch array was printed on the top side of the substrate, and the feeding structure, which is an open-ended leaky-wave slot line, was etched on the bottom side of the substrate. The antenna performed as a Fabry-Perot cavity antenna at high thickness levels ($H=160{\mu}m$ and $H=80{\mu}m$), thus exhibiting high gain but a narrow gain bandwidth. At low thickness levels ($H=40{\mu}m$ and $H=20{\mu}m$), it performed as a metasurface antenna and showed wide-gain-bandwidth characteristics with a low gain value. Aside from the advantage of achieving useful characteristics for different antennas by just changing the substrate thickness, the proposed antenna design exhibited a low profile, easy integration into circuit boards, and excellent low-cost mass production suitability.

Sorafenib-triggered radiation recall dermatitis with a disseminated exanthematous reaction

  • Oh, Dongryul;Park, Hee Chul;Lim, Ho Yeong;Yoo, Byung Chul
    • Radiation Oncology Journal
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    • 제31권3호
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    • pp.171-174
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    • 2013
  • Sorafenib is a multi-targeted kinase inhibitor, which is the current standard treatment for advanced hepatocellular carcinoma (HCC). Only one case of radiation recall dermatitis (RRD) associated with sorafenib has been reported so far. Our patient with recurrent HCC was treated with palliative radiotherapy (RT) for the chest wall mass. Sorafenib at 400 mg twice daily was begun on the day following RT. On the 14th day post-RT, an erythematous patch was observed on right chest wall which matched area previously irradiated. It was consistent with RRD. Ten days later, a disseminated exanthematous rash and severe pruritus occurred. Sorafenib was stopped and an oral antihistamine was prescribed to relieve symptoms. At the 1-week follow-up after the cessation of sorafenib, all symptoms were resolved. Physicians should be alert to this recall phenomenon as it can occur both in the skin and elsewhere and the occurrence of RRD may be unpredictable.

원발성 심장종양에 대한 외과적 치험 (Surgical Treatment of Primary Cardiac Tumor)

  • 차경태
    • Journal of Chest Surgery
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    • 제24권7호
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    • pp.701-711
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    • 1991
  • We experienced 6 cases of primary cardiac tumor, all received operation for removal of tumor. Mean age was 43.8 years-old ranging from 17 years-old to 66 years-old. Five cases were female, one case was male. Five cases were benign, myxoma, all located within left atrium. One case was malignant, angiosarcoma within right atrium. All patient showed cardiac manifestations. One case was in NYHA functional class II, two were in III, three were in IV. Four patients showed constitutional symptoms, but no one showed evidence of embolic phenomenon. All case of myxoma showed cardiomegaly except one malignancy. Only one case was regular sinus rhythm, three were sinus tachycardia 8z two were atrial fibrillation. The most common site of tumor origin was fossa ovalis limbus[four of all]. Two of five myxomas received emergency operation, one patient died postoperatively. Lived four patients showed no evidence of recurrence[mean follow-up, 3,5 years], but one patient has Grade II /IV mitral regurgitation & in OPD follow-up now, One malignant case, 17 years-old cerebral palsy female, was angiosarcoma occupied most of right atrial chamber originated from anterior wall of right atrium, received emergency operation which was removal of mass & reconstruction of right atrium with artificial pericardial patch. This patient died on postoperative 36th day due to persistent LCOS[low cardiac output syndrome] with combined sepsis.

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우관상동맥 폐색을 초래한 심근 농양 -1례 보고- (Myocardial Abscess with Coronary Artery Occlusion -One Case Report)

  • 이재익;김기봉
    • Journal of Chest Surgery
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    • 제30권8호
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    • pp.823-826
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    • 1997
  • 심근 농양은 대개 감염성 심내막염이나 패혈증의 합병증으로 생길 수 있다. 심근 농양이 관상 동맥을 압박 하여 심근 허혈을 초래한 경우는 1987년 Cripps 등이 보고한 이래 5-6례 있을뿐이다. 61세 남자 환자가 내원 6주 전부터 시작된 원인을 알 수 없는 발열과 오한을 주소로 내원하였다. 환자는 발열이 시작된지 2주후에 심실 세동 및 이로 인한 심장 마비로 심폐소생술을 시행받은 병력이 있었다. 심에코와 관상동맥 조영 결과 우측 방실구 부위의 심근 농양이 우관상동맥을 외부에서 압박하면서 심근 경색을 초래한 소견을 보였다. 수 술은 농양을 변연 절제하였으며 괴사된 심방벽을 절제한 후 생긴 결손은 자가 심낭을 이용한 patch로 폐쇄하 였고 우측 내유동맥을 우관상동맥의 원위부에 문합하였다. 환자는 합병증없이 퇴원하였으며 수술 중 검체에 서 시행한 농양배양 검사에서는 Salmonella arizona가 동정되었다.

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