1.Identification of Compound Heterozygous EYS Variants in a Korean Patient with Retinitis Pigmentosa.
Hyoung Tae KIM ; Ja Hyun JANG ; Kyungeun KANG ; Chang Seok KI ; Hyewon CHUNG
Laboratory Medicine Online 2018;8(2):66-70
No abstract available.
Humans
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Retinitis Pigmentosa*
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Retinitis*
2.MUC2 Expression Is Correlated with Tumor Differentiation and Inhibits Tumor Invasion in Gastric Carcinomas: A Systematic Review and Meta-analysis.
Jung Soo PYO ; Jin Hee SOHN ; Guhyun KANG ; Dong Hoon KIM ; Kyungeun KIM ; In Gu DO ; Dong Hyun KIM
Journal of Pathology and Translational Medicine 2015;49(3):249-256
BACKGROUND: While MUC2 is expressed in intestinal metaplasia and malignant lesions, the clinicopathological significance of MUC2 expression is not fully elucidated in gastric carcinoma (GC). METHODS: The present study investigated the correlation between MUC2 expression and clinicopathological parameters in 167 human GCs. In addition, to confirm the clinicopathological significance of MUC2 expression, we performed a systematic review and meta-analysis in 1,832 GCs. RESULTS: MUC2 expression was found in 58 of 167 GCs (34.7%). MUC2-expressing GC showed lower primary tumor (T), regional lymph node (N), and tumor node metastasis (TNM) stages compared with GCs without MUC2 expression (p=.001, p=.001, and p=.011, respectively). However, MUC2 expression was not correlated with Lauren's classification and tumor differentiation. In meta-analysis, MUC2 expression was significantly correlated with differentiation and lower tumor stage (odds ratio [OR], 1.303; 95% confidence interval [CI], 1.020 to 1.664; p = .034 and OR, 1.352; 95% CI, 1.055 to 1.734; p = .017, respectively) but not with Lauren's classification, pN stage, or pTNM stage. CONCLUSIONS: MUC2 expression was correlated with a lower tumor depth and lower lymph node metastasis in our study; the meta-analysis showed a correlation of MUC2 expression with tumor differentiation and lower tumor depth.
Classification
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Humans
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Lymph Nodes
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Metaplasia
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Neoplasm Metastasis
3.Extranodal Follicular Dendritic Cell Sarcoma with Rapid Growth in Parapharynx: A Case Report.
Jung Soo PYO ; Guhyun KANG ; Sung Im DO ; Seoung Wan CHAE ; Kyungeun KIM ; Sang Hyuk LEE ; Yoon La CHOI ; Joon Hyuk CHOI ; Jin Hee SOHN ; Dong Hoon KIM
Korean Journal of Pathology 2012;46(3):306-310
Follicular dendritic cell sarcoma (FDCS) is a rare malignancy arising from the antigen-presenting cells in the lymph node and extranodal tissue. We describe a 31-year-old male patient who presented with a swelling of the left parapharynx. The radiologic findings showed a 4.7x4.5x1.9 cm-sized, ill-defined mass in the left parapharyngeal space. A fine-needle aspiration cytology was performed and it showed scattered, irregular, cohesive clusters of tumor cells with a spindle-to-ovoid shape with irregular contours in a background of lymphocytes. Based on these findings, a diagnosis of spindle cell neoplasm was made. The surgically resected tumor was composed of elongated, ovoid or polygonal cells showing positive immunohistochemistry for CD21, CD23, and CD35. Postoperatively, the residual tumor was observed to undergo a rapidly growth. There is an overlap in the cytologic and histologic findings between FDCS of the parapharynx and other tumors. Pathologists should therefore be aware of its characteristics not only to provide an accurate diagnosis but also to recommend the appropriate clinical management.
Male
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Humans
4.Extranodal Follicular Dendritic Cell Sarcoma with Rapid Growth in Parapharynx: A Case Report.
Jung Soo PYO ; Guhyun KANG ; Sung Im DO ; Seoung Wan CHAE ; Kyungeun KIM ; Sang Hyuk LEE ; Yoon La CHOI ; Joon Hyuk CHOI ; Jin Hee SOHN ; Dong Hoon KIM
Korean Journal of Pathology 2012;46(3):306-310
Follicular dendritic cell sarcoma (FDCS) is a rare malignancy arising from the antigen-presenting cells in the lymph node and extranodal tissue. We describe a 31-year-old male patient who presented with a swelling of the left parapharynx. The radiologic findings showed a 4.7x4.5x1.9 cm-sized, ill-defined mass in the left parapharyngeal space. A fine-needle aspiration cytology was performed and it showed scattered, irregular, cohesive clusters of tumor cells with a spindle-to-ovoid shape with irregular contours in a background of lymphocytes. Based on these findings, a diagnosis of spindle cell neoplasm was made. The surgically resected tumor was composed of elongated, ovoid or polygonal cells showing positive immunohistochemistry for CD21, CD23, and CD35. Postoperatively, the residual tumor was observed to undergo a rapidly growth. There is an overlap in the cytologic and histologic findings between FDCS of the parapharynx and other tumors. Pathologists should therefore be aware of its characteristics not only to provide an accurate diagnosis but also to recommend the appropriate clinical management.
Male
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Humans