• 제목/요약/키워드: Clear Cell

검색결과 771건 처리시간 0.028초

나선식 CT를 이용한 혐색소형 신세포암과 투명세포형 신세포암의 감별 (Differentiation of Chromophobe Renal Cell Carcinoma and Clear Cell Renal Cell Carcinoma by Using Helical CT)

  • 김홍철;조재호
    • Journal of Yeungnam Medical Science
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    • 제29권1호
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    • pp.14-18
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    • 2012
  • Background: The purpose of this study was to differentiate chromophobe renal cell carcinoma and clear cell renal cell carcinoma on helical CT. Methods: The CT images of 9 patients histopathologically proven to have chromophobe renal cell carcinoma and 20 patients with clear cell renal cell carcinoma were reviewed. The tumor sizes, margins, enhancement degrees and patterns, presence or absence of calcification, and tumor spread patterns (including perinephric changes, venous invasion, lymphadenopathy, and distant metastasis) were compared. Results: All the chromophobe renal cell carcinomas showed well-demarcated margins. Thechromophobe renal cell carcinomas showed milder enhancements than the clear cell renal cell carcinomas. The sensitivity and specificity for differentiating the chromophobe renal cell carcinoma from the clear cell renal cell carcinoma were 100 and 88%, respectively, when 101 Hounsfield units was used as the cut-off value in the corticomedullary phase, and 95 and 100% when a less-than-three-time enhancement change was used as a cut-off value in the corticomedullary phase (p<0.05). The chromophobe renal cell carcinomas (67%) tended to show a homogeneous enhancement whereas the clear cell renal cell carcinomas (85%) usually showed a heterogeneous enhancement (p<0.05). Statistical analysis revealed that the frequencies of the tumor spread pattern and calcification in the two subtypes didnot differ significantly (p>0.05). Conclusion: The CT findings of the chromophobe renal cell carcinomascompared to those of the clear cell renal cell carcinomas showed that there were mild enhancements in the corticomedullary phase, homogeneous enhancements, and well-demarcated margins.

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유방의 당원성 투명세포암종의 세침흡인 세포학적 소견 - 2예 보고 - (Fine Needle Aspiration Cytology of Glycogen-Rich Clear Cell Carcinoma of the Breast - A Report of 2 Cases -)

  • 김완섭;이원미;홍은경;박문향;이중달
    • 대한세포병리학회지
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    • 제9권2호
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    • pp.213-219
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    • 1998
  • Glycogen-rich clear ceil carcinoma of the breast is an unusual variant of carcinoma with a recorded incidence of $1.4{\sim}3%$ of breast carcinomas. The cytologic characteristics have not been well described. We report two cases of glycogen-rich clear cell carcinoma with corresponding fine needle aspiration(FNA) cytologic findings and compare them to infiltrating ductal carcinoma and other clear ceil malignancies with a review of literature. One was a 62-year-old woman exhibiting a palpable mass of the right breast. The smears showed atypical tight cell clusters and individually scattered single cells containing leanly or clear abundant cytoplasm with well defined cytoplasmic margins. Mild to moderate nuclear pleomorphism and a prominent nucleolus were present. The other was a 42-year-old woman who was admitted with a right breast mass. The smears showed moderately cellular, tightly cohesive tumor cells. The cytoplasmic outline was generally well demarcated. The tumor cells Contained foamy to clear abundant cytoplasm with large and small vacuoles. The nuclear pleomorphism was marked. Both tumors resected by modified radical mastectomy, were diagnosed as glycogen-rich clear cell carcinoma. Histologically, the clear cell nature of tumor cells were not characteristic enough to predict this type of the tumor. Some cytologic features can be distinguished other clear cell breast cancer from glycogen-rich carcinoma. Recognition of these unusual patterns in a breast FNAC should raise the suspicion of a clear cell carcinoma including glycogen-rich subtype. Cytological localization of glycogen using PAS and D-PAS staining may permit the correct Identification and differential diagnosis of this tumor.

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악성 한선종의 초음파 소견: 증례 보고 (Ultrasonography of Malignant Clear Cell Hidradenoma: A Case Report)

  • 함태혁;천상진;노미숙;하동호
    • 대한영상의학회지
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    • 제81권2호
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    • pp.448-452
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    • 2020
  • 한선종은 땀샘에서 기원하는 종양으로 전형적으로 진피 및 피하층에 위치한다. 악성 한선종은 매우 드물다. 그리고, 보통 영상 검사 없이 수술적 절제 치료를 시행한다. 악성 한선종의 초음파 소견도 매우 드물게 보고되어 있다. 저자들은 악성 한선종의 초음파 소견을 보고하고자 한다.

경부에 재발한 투명세포땀샘종의 치료에 대한 증례 보고 (A Treatment of Recurrent Clear Cell Hidradenoma on the Neck: A Case Report)

  • 김순제;양희상;신정민;오상하
    • 대한두경부종양학회지
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    • 제36권2호
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    • pp.41-44
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    • 2020
  • Clear cell hidradenoma is a skin adnexal tumor originating from eccrine glands. The risk of local recurrence after surgical resection exceeds 50%, and 6-19% of cases are malignant. The rarity of clear cell hidradenoma and its diverse histological findings make this type of tumor a diagnostic challenge. We present a case of recurrent clear cell hidradenoma of the posterior neck in a 70-year-old woman. The tumor recurred once after complete excision, and did not recur again after 1-cm wide excision and reconstruction with a local bilobed flap. Recurrent clear cell hidradenomas are activated by surgical stimulation, increasing the risk for metastasis. Therefore, we suggest that wide excision with confirmation of a tumor-free margin by frozen-section biopsy should be the first-line treatment for recurrent benign clear cell hidradenoma.

혀 기저부에 발생한 투명세포암종 1예 (A Rare Case of Clear Cell Carcinoma of the Tongue Base: A Case Report)

  • 김홍진;;오화은;오경호;권순영
    • 대한두경부종양학회지
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    • 제40권1호
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    • pp.15-17
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    • 2024
  • Clear cell carcinoma is a rare variant of salivary gland carcinoma, and its occurrence in the tongue base is even rarer. We present a case of a 55-year-old female patient with clear cell carcinoma of the tongue base. The patient initially presented with a 3-month history of palpable tongue mass, leading to her visit to the otolaryngology outpatient clinic. The patient underwent a complete resection of the tumor under general anesthesia. Postoperative follow-up imaging studies showed no evidence of recurrence. This case report highlights the diagnostic and management challenges associated with clear cell carcinoma of tongue base and demonstrates that a high index of suspicion is required to diagnose clear cell caricnoma, given its rarity and overlapping features with other clear cell neoplasms.

난소의 원발 투명세포암종의 세포소견 (Cytologic Findings of Clear Cell Carcinoma of Ovary)

  • 박지영;김혜선;최종순
    • 대한세포병리학회지
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    • 제17권1호
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    • pp.32-37
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    • 2006
  • The objective of this study was to evaluate the cytomorphologic features of histologically confirmed clear cell carcinoma of the ovary and to evaluate the applicability of scrape or fine-needle aspiration cytology in making an intraoperative diagnosis. We reviewed scrape or fine-needle aspiration cytology findings in tissues taken from 6 patients with clear cell carcinoma of the ovary. The cytologic diagnosis was based primarily on findings in alcohol-fixed, hematoxylin-eosin (H-E) stained smears. The formation of material resembling a basement membrane was a characteristic finding in these smears. This extracellular hyaline material was stained light pink with H-E and was frequently found within tumor cell clusters as well as in the background material. Multinucleated giant cells were found occasionally. Each tumor cell had an abundant, clear, or granular cytoplasm with a distinct cellular membrane. Scrape cytology is a simple and rapid supportive method and could be helpful in diagnosing clear cell carcinoma of the ovary, especially when marked artifacts appear in the frozen section.

소아의 수부골에 전이된 신장의 투명세포육종 -1례 보고- (Metastatic Clear Cell Sarcoma of the Kidney in a Child's Hand Bone - A Case Report -)

  • 심종섭;김지형;서연림
    • 대한골관절종양학회지
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    • 제4권2호
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    • pp.94-98
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    • 1998
  • Clear cell sarcoma of the kidney (CCSK) is a rare malignant tumor of the renal origin in childhood, distinguished from Wilms tumor by its pathologic and clinical features. Bone metastasis is one of the characteristic clinical features. The common site of metastasis of the clear cell Sarcoma of the kidney is axial skeleton including skull, spines, ribs and femur. A cases of clear cell Sarcoma of the kidney presented to us, which solely metastasized to the hand bones without metastasizing to any other tissues including axial skeleton. We report this case with review of literatures.

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자궁경부 투명세포 샘암종의 자궁경부질 세포학적 소견 - 1예 보고 - (Cytology of the Uterine Cervico-vaginal Smear of Clear Cell Adenocarcinoma in Uterine Cervix - Report of a Case -)

  • 맹이소;김경미;강창석;이안희
    • 대한세포병리학회지
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    • 제15권2호
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    • pp.116-119
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    • 2004
  • Primary clear cell adenocarcinoma of uterine cervix is rare and cytomorphology in the vaginal smear have not been previously described in Korean literatures. The cytologic characteristics of clear cell adenocarcinoma of the uterine cervix include : malignant cells with abundant, finely vacuolated cytoplasm ; hobnail appearance, and distinctive basement membrane-like hyaline materials within cellular aggregates. A 36-year-old woman presented with vaginal bleeding. Cytologic examination of vaginal smear and histopathologic examination of a radical hysterectomy specimen allowed the diagnosis of hemorrhagic tumor in the uterine cervix as a clear cell adenocarcinoma. Cytologic findings were very characteristic. The tumor cells had abundant, pale, finely vacuolated cytoplasm with indistinct cytoplasmic membrane. The nuclei were round to oval with finely dispersed chromatin. Extracellular basement membrane-like hyaline substance, which stained a light green color in Papanicolaou's preparation, was frequently observed within the cancer cell clusters.

Clear Cell Sarcoma of the Wrist: MRI Findings with Diffusion-Weighted Image and Histopathologic Correlation

  • Chung, Bo Yong;Lee, Seun Ah;Choi, Jung-Ah;Shim, Jung-Weon
    • Investigative Magnetic Resonance Imaging
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    • 제20권2호
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    • pp.136-139
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    • 2016
  • Clear cell sarcoma is rare and difficult to diagnose. Herein, we present a case of clear cell sarcoma in the dorsum of the wrist with MRI findings, including diffusion-weighted imaging, and histopathologic correlation, which was initially diagnosed as giant cell tumor of tendon sheath.

Thoracic Intramedullay Clear Cell Meningioma

  • Kim, Min-Seok;Park, Seong-Hyun;Park, Yeun-Mook
    • Journal of Korean Neurosurgical Society
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    • 제39권5호
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    • pp.389-392
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    • 2006
  • Intramedullary clear cell meningioma[CCM]. which is more aggressive than other variants of meningioma, is extremely rare. To date, only one case has been documented in spinal tumors. We report the first case of an intramedullary CCM originating in the spinal cord at the thoracic region.