• 제목/요약/키워드: tissue cyst

검색결과 232건 처리시간 0.032초

Expression and secretion of CXCL12 are enhanced in autosomal dominant polycystic kidney disease

  • Kim, Hyunho;Sung, Jinmo;Kim, Hyunsuk;Ryu, Hyunjin;Park, Hayne Cho;Oh, Yun Kyu;Lee, Hyun-Seob;Oh, Kook-Hwan;Ahn, Curie
    • BMB Reports
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    • 제52권7호
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    • pp.463-468
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    • 2019
  • Autosomal dominant polycystic kidney disease (ADPKD), one of the most common human monogenic diseases (frequency of 1/1000-1/400), is characterized by numerous fluid-filled renal cysts (RCs). Inactivation of the PKD1 or PKD2 gene by germline and somatic mutations is necessary for cyst formation in ADPKD. To mechanistically understand cyst formation and growth, we isolated RCs from Korean patients with ADPKD and immortalized them with human telomerase reverse transcriptase (hTERT). Three hTERT-immortalized RC cell lines were characterized as proximal epithelial cells with germline and somatic PKD1 mutations. Thus, we first established hTERT-immortalized proximal cyst cells with somatic PKD1 mutations. Through transcriptome sequencing and Gene Ontology (GO) analysis, we found that upregulated genes were related to cell division and that downregulated genes were related to cell differentiation. We wondered whether the upregulated gene for the chemokine CXCL12 is related to the mTOR signaling pathway in cyst growth in ADPKD. CXCL12 mRNA expression and secretion were increased in RC cell lines. We then examined CXCL12 levels in RC fluids from patients with ADPKD and found increased CXCL12 levels. The CXCL12 receptor CXC chemokine receptor 4 (CXCR4) was upregulated, and the mTOR signaling pathway, which is downstream of the CXCL12/CXCR4 axis, was activated in ADPKD kidney tissue. To confirm activation of the mTOR signaling pathway by CXCL12 via CXCR4, we treated the RC cell lines with recombinant CXCL12 and the CXCR4 antagonist AMD3100; CXCL12 induced the mTOR signaling pathway, but the CXCR4 antagonist AMD3100 blocked the mTOR signaling pathway. Taken together, these results suggest that enhanced CXCL12 in RC fluids activates the mTOR signaling pathway via CXCR4 in ADPKD cyst growth.

선천성 낭포성 선양기종: 1례 보고 (Congenital Cystic Adenomatoid Malformation of The Lung - A Case Report -)

  • 김명인
    • Journal of Chest Surgery
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    • 제24권8호
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    • pp.819-823
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    • 1991
  • The congenital cystic adenomatoid malformation of the lung is a rare disease, and is one of the most common congenital lung diseases which require prompt surgical intervention. The prognosis depends on its tissue type, prompt diagnosis and surgical intervention. The lesion consists of enlarged, variable sized multiple cyst with overgrowth of terminal bronchioles, like hamartoma. This disease can be associated with other vascular anomalies or other congenital defect especially in type II lesion We recently experienced one case of congenital cystic adenomatoid malformation The patient was 2 months old infant who showed respiratory distress without associated anomaly. After right upper lobe lobectomy, the patient was recovered uneventfully.

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Parotid mandibular bone defect: A case report emphasizing imaging features in plain radiographs and magnetic resonance imaging

  • Hisatomi, Miki;Munhoz, Luciana;Asaumi, Junichi;Arita, Emiko Saito
    • Imaging Science in Dentistry
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    • 제47권4호
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    • pp.269-273
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    • 2017
  • Mandibular bone depression, also known as Stafne bone cavity, is defined as a bone depression filled mainly with salivary gland tissue. Parotid gland bone defects are infrequently observed. We report the case of a 52-year-old male patient who underwent radiographic examinations due to temporomandibular joint dysfunction, and a radiolucent area was detected in the mandibular ramus, with a provisional diagnosis of traumatic bone cyst or parotid mandibular bone defect. The patient was then referred for magnetic resonance imaging, which demonstrated a hyperintense area eroding the mandibular ramus, which corresponded to glandular tissue. Although the defect was a benign lesion, radiolucencies in the mandibular ramus lead to concerns among professionals, because their radiographic features can resemble various intrabony neoplastic lesions, such as giant cell tumors or benign tumors of the parotid gland.

하악골에 발생한 근섬유종: 증례 보고 (Myofibroma of the mandible: A case report)

  • 김진수;김성은;김재덕
    • Imaging Science in Dentistry
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    • 제36권4호
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    • pp.211-215
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    • 2006
  • Myofibroma is a rare benign soft tissue tumor that in all ages usually occurs in the head and neck region, and at subcutaneous tissue, but rarely has bone origin within bone. Intraosseous lesions are more often found in childhood. Although intraosseous lesions are relatively common in mandible. Reports for mandible, reports on radiographic findings of myofibroma occurred on the mandible are uncommon. We describe the radiographic appearance on the conventional radiographs and CT of myofibroma of the mandible in a 9-year-old boy. This benign lesion closely resembles to odontogenic cyst or tumor on image.

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복부 피하지방조직의 폐흡충증 이소기생례 (A case of paragonimiasis in the abdominal subcutaneous tissue)

  • 최원영;정상설
    • Parasites, Hosts and Diseases
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    • 제29권4호
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    • pp.407-410
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    • 1991
  • 서울에 거주하는 36세의 가정주부가 복부의 종류로 인해 내원하였다. 국소마취 하에 복부의 피하지방층에 있는 종류를 제거하여 지름 3 cm정도의 낭과 그 속에 7×4 mm크기의 충체를 얻었다. 이 환자는 생선회를 즐겨 먹은 과거적이 있었으며 충체를 acetocarmine 염색하여 관찰한 결과 폐흡충으로 동정하여 이에 폐흡충중의 이소기생례를 보고하는 바이다.

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기관지 낭종의 전산화단층촬영 소견 (CT Findings of Bronchogenic Cyst)

  • 조현철;이용우;황미수;조길호;변우목;조재호;장재천;박복환
    • Journal of Yeungnam Medical Science
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    • 제12권2호
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    • pp.226-236
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    • 1995
  • 이 연구의 목적은 기관지낭종의 CT소견을 분석하여 그 특징을 알아보고자 하였다. 수술후 조직학적으로 기관지낭종으로 확진된 11명의 CT소견을 후향적으로 분석하였다. 전 예에서 조영증강 전 후의 CT가 시행되었고 CT상 병변의 위치, 크기, CT 음영과 조영증강 정도, 석회화 유무 등을 중심으로 분석하였다. 총 11례중 3례는 폐실질내에 8례는 종격동내에 위치하였다. 폐실질내 기관지낭종 3례중 2례는 우하엽, 1례는 좌하엽에 위치하였고 평균 크기는 9.7 cm이었다. CT상 1례는 공기로만 찬 낭포, 1례는 균질한 물음영의 낭종, 1례는 공기방울을 가지는 고음영의 낭종으로 보였다. 종격동내 기관지낭종 8례 중 5례는 후종격동, 2례는 상종격동, 1례는 중종격동에 위치하였으며 평균 크기는 5.0 cm이었다. CT상 5례는 균질한 물음영으로 나타났고, 1례는 공기수면상을 보였으며, 2례는 근육과 비슷한 정도의 고음영으로 나타났고 그중 1례는 65 HU를 보였다. 모든 예에서 석회화나 조영증강은 보이지 않았다. 수술소견상 폐실질내 기관지낭종은 3례 모두에서 낭종내에 지저분한 농양의 액체를 가지고 있었고 종격동내 기관지낭종은 8례 모두에서 희거나 노란색의 점액질 액체를 보였다. 기관지낭종은 균일한 물음영을 보이는 경우가 가장 많으며, 그 외 근육과 비슷한 정도의 고음영, 공기수면상, 공기로만 찬 낭포 등으로 보였으며 이와 같은 소견은 기관지낭종의 진단과 감별에 도움이 될 것으로 생각한다.

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아래 눈꺼풀에서 발생한 지방 경화성 육아종의 치험례 (A Case of Liposclerosing Granuloma Arising from Lower Eyelid)

  • 박보영;강소라
    • Archives of Plastic Surgery
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    • 제35권5호
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    • pp.603-606
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    • 2008
  • Purpose: Sclerosing lipogranuloma is an unusal benign condition of the genitalia following injections into the genitalia with exogenous paraffin or mineral oil. A few cases have been reported in which sclerosing lipogranuloma of the lid was caused by paraffin-containing ointment plugs after the endonasal sinus surgery. A 52-year-old man presented with a painless hard mass of the right lower lid after the MRI scan at the Ophthalmology department. Nine months before, he had undergone right maxilla sinus surgery through the oral incision. And he was also gotten nasal packing with Vaseline gauze after the surgery. Methods: The round shaped two masses in the Right lower lid were approximately $1.0{\times}1.0cm$ in size. There were no size or color change, bleeding and ulceration. The MRI scan showed a suspicious part of an abscess of benign tumor. Also, He was planned cyst remove through the endonasal surgery due to the mucoid cyst in the right maxillary sinus in the ENT dept. Under the general anesthesia, the patient underwent surgical excision through a subcilliary incision with endonasal sinus surgery. The masses were in deep subcutaneous orbital fat with no connection with right maxillary sinus. Results: The masses were excised $2.1{\times}0.7cm$ in size including surrounding necrotic fatty tissue. Histopathological diagnosis was 'sclerosing lipogranuloma' due to paraffin or similar substance with fat necrosis and cystic change. This tissue was positive in PAS, S-100, CD68 reaction. Conclusion: It is extremely rare to find a granulomatous orbital lesion arising to a endonasal surgery. In conclusion, if sclerosing lipogranuloma is suspected excisional biopsy should be undertaken. Surgery should be reserved for recurrent or refractory cases when steroids have failed as first-line treatment at the 6-month follow-up examination, There was no complication or recurrence.

소아의 이소성 경부흉선 1예 (A Case of Aberrant Cervical Thymus in a One-year-old Boy)

  • 이성철;양석진;김우기
    • Advances in pediatric surgery
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    • 제2권1호
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    • pp.64-67
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    • 1996
  • 1세된 남아에서 세열낭종을 의심한 좌측 경부 종양이 수술을 시행한 결과 고형종양이였고, 조직검사상 이소성 흉선으로 판명되었다. 술후 초음파상 흉선은 정상적으로 있었고, 현재 환자의 면역기능은 아무 이상없이 정상으로 자라고 있다.

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근골격계 초음파검사가 도움이 되는 진료 상황 (Clinical Situations in which Musculoskeletal Ultrasound is Helpful)

  • 조길호
    • Journal of Yeungnam Medical Science
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    • 제18권2호
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    • pp.170-186
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    • 2001
  • Musculoskeletal ultrasound (MSUS) has newly evolved by the mechanical improvement of the machine over past several years, becoming a part of imaging techniques for the evaluation of variable diseases in the musculoskeletal system. MSUS has proven diagnostic superiority in pathologies including rotator cuff disease of the shoulder, lateral epicondylitis of the elbow, diseases of the peripheral nerve, detection of intra-articular loose bodies and soft tissue foreign bodies, and in evaluating small superficial soft tissue tumors such as ganglion, epidermoid cyst, and glomus tumor. Besides, MSUS is very useful for obtaining tissue or fluid via percutaneous fine needle aspiration and/or biopsy for the histopathologic diagnosis. Combining MSUS with MR would play a great role in the field of the diagnostic imaging of the musculoskeletal system. The MSUS examiner should have the knowledge of cross-sectional anatomy, and of the mechanical and physical properties of ultrasound in order to interpret the ultrasound findings accurately and properly, and to avoid diagnostic errors due to variable artifacts subsequently. The goal of this article is to introduce the capabilities of MSUS in certain kinds of clinical situation and to familiarize the reader with MSUS. For the purpose, author intends to describe this article according not to the disease-, or organ-based, but to the clinical problem-based format.

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전이성 선암종을 포함한 경부하마종(Plunging ranula)의 치험례 (A CASE REPORT OF PLUNGING RANULA WITH METASTATIC ADENOCARCINOMA)

  • 정해석;팽준영;명훈;김명진
    • Journal of the Korean Association of Oral and Maxillofacial Surgeons
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    • 제33권5호
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    • pp.543-547
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    • 2007
  • The plunging ranula is a kind of ranula that goes over the mouth floor to the neck and other adjacent tissue. Sublingual gland is gently accepted as origin of plunging ranula. Plunging ranula develops commonly because of rupture of sublingual gland duct by trauma and extravasation of salivary secretion to the adjacent tissue. It is not true cyst so that there is no epithelium. And it consisted with thin connective tissue, inflammation cell infiltration and salivary secretion. Left without treatment, it can grow into the 10 cm more huge lesion. This report is a case of 73 years old female who was diagnosed as plunging ranula with review of literature. She presented 5 cm submandibular swelling at first. When surgery was delayed because of patient's condition, the lesion grew into the l2cm huge size. We performed excision of sublingual gland, submandibular gland and plunging ranula and had a good result without recurrence.