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Case Study
Multicystic Biliary Hamartoma of the Liver
Ji Soo Song, Sang Jae Noh, Baik Hwan Cho, Woo Sung Moon
Korean J Pathol. 2013;47(3):275-278.   Published online June 25, 2013
DOI: https://doi.org/10.4132/KoreanJPathol.2013.47.3.275
  • 7,234 View
  • 75 Download
  • 15 Crossref
AbstractAbstract PDF

Multicystic biliary hamartoma (MCBH) is a very rare hamartomatous cystic nodule of the liver, which has recently been described as a new entity of a hepatic nodular lesion. We report a unique case of MCBH with a review of the literatures. A hepatic multicystic mass of segment 3 was detected in a 52-year-old male by abdominal computed tomography, and resection of this lesion was performed. Macroscopic examination revealed a 2.7×2.0 cm nodular mass with a multicystic honeycomb cut surface. Histologically, this lesion consisted of multiple dilated cystic ducts lined by biliary type epithelial cells, periductal glands and connective tissue, which included small amounts of hepatic parenchyma and blood vessels. Recognition of this unusual lesion is essential to avoid confusion with other cystic tumors of the liver, and to learn more about its natural history and response to treatment.

Citations

Citations to this article as recorded by  
  • Technical Considerations in EEG Source Imaging
    Benjamin H. Brinkmann
    Journal of Clinical Neurophysiology.2024; 41(1): 2.     CrossRef
  • A Case of Multicystic Biliary Hamartoma with a Marked Peribiliary Gland Component Successfully Treated by Purely Laparoscopic Anatomical Liver Resection
    Keita Kai, Takao Ide, Tomokazu Tanaka, Kumpei Yukimoto, Hiroyuki Irie, Hirokazu Noshiro, Shinichi Aishima
    Journal of Gastrointestinal Cancer.2023; 54(3): 996.     CrossRef
  • Characteristics of multicystic biliary hamartoma: A case report
    Jia Lian, Lixia Sun, Yankai Yang, Jun Li, Ye Zhang, Guiqiu Liu, Weijuan Hu
    Frontiers in Surgery.2023;[Epub]     CrossRef
  • Hamartoma multiquístico de vías biliares
    Victoria Carmona, Iago Justo, Yolanda Rodríguez-Gil, Alberto Marcacuzco, Carmelo Loinaz, Carlos Jiménez
    Cirugía Española.2022; 100(12): 800.     CrossRef
  • Multicystic Biliary Hamartoma With Xanthogranulomatous Inflammation on 18F-FDG PET/CT
    Nahomi Shono, Yoichi Otomi, Hideki Otsuka, Takayoshi Shinya, Masafumi Harada
    Clinical Nuclear Medicine.2022; 47(10): 882.     CrossRef
  • Intrahepatic multicystic biliary hamartoma: A case report
    Chen-Yu Wang, Fu-Yang Shi, Wei-Feng Huang, Yan Tang, Ting Li, Guo-Lin He
    World Journal of Clinical Cases.2022; 10(26): 9361.     CrossRef
  • A Case of Multicystic Biliary Hamartoma Treated with Left Medial Sectionectomy
    Naomi KUROKI, Tomoaki TANAKA, Takanobu SUGASE, Syoji TANIGUCHI, Takashi GOTO, Rintaro KOGA, Takumi KIWAKI, Hiroyuki TANAKA
    Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2022; 83(2): 395.     CrossRef
  • Multicystic biliary hamartoma
    Victoria Carmona, Iago Justo, Yolanda Rodríguez-Gil, Alberto Marcacuzco, Carmelo Loinaz, Carlos Jiménez
    Cirugía Española (English Edition).2022; 100(12): 800.     CrossRef
  • Case Report: Incidentally Discovered a Rare Cystic Lesion of Liver: Multicystic Biliary Hamartoma
    Wentao Mu, Peng Su, Shanglei Ning
    Pathology and Oncology Research.2021;[Epub]     CrossRef
  • Bile Duct Hamartoma Mimicking Liver Metastasis in Suspected Porcelain Gallbladder: a Case Report
    Gautham Krishnamurthy, Harjeet Singh, Sravya Deepika Ganti, Ganga Ram Verma
    Journal of Gastrointestinal Cancer.2019; 50(4): 1022.     CrossRef
  • A variant of multicystic biliary hamartoma presenting as an intrahepatic cystic neoplasm
    Tetsuro Tominaga, Takafumi Abo, Naoe Kinoshita, Tomonori Murakami, Yasunori Sato, Yasuni Nakanuma, Kenich Harada, Junichi Masuda, Takeshi Nagayasu, Atsushi Nanashima
    Clinical Journal of Gastroenterology.2015; 8(3): 162.     CrossRef
  • Hamartoma biliar multiquístico intrahepático: presentación de un caso clínico
    María Jezabel Fernández-Carrión, Ricardo Robles Campos, Asunción López Conesa, Roberto Brusadín, Pascual Parrilla Paricio
    Cirugía Española.2015; 93(9): e103.     CrossRef
  • Intrahepatic Multicystic Biliary Hamartoma: Presentation of a Case Report
    María Jezabel Fernández-Carrión, Ricardo Robles Campos, Asunción López Conesa, Roberto Brusadín, Pascual Parrilla Paricio
    Cirugía Española (English Edition).2015; 93(9): e103.     CrossRef
  • Multicystic biliary hamartoma: A report of a rare entity and a review of the literature
    Rachel E. Beard, Eric U. Yee, Koenraad J. Mortele, Khalid Khwaja
    International Journal of Surgery Case Reports.2014; 5(12): 919.     CrossRef
  • Multicystic biliary hamartoma mimicking intrahepatic cholangiocarcinoma: report of a case
    Tomoaki Yoh, Ryuji Okamura, Hiroyuki Nakayama, Xue Lin, Yuya Nakamura, Tatsushi Kato
    Clinical Journal of Gastroenterology.2014; 7(5): 418.     CrossRef
Case Reports
Simultaneous Pancreatic Serous Microcystic Adenoma and Intraductal Papillary Mucinous Tumor of the Pancreas: A Case Report.
Hyoung Jong Kwak, Young Kon Kim, Baik Hwan Cho, Woo Sung Moon
Korean J Pathol. 2011;45:S29-S31.
DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.S1.S29
  • 2,685 View
  • 22 Download
AbstractAbstract PDF
Serous cystadenomas of the pancreas account for approximately a third of pancreatic cystic neoplasms. Their coexistence with a second tumor is extremely rare. We now report a case of a serous microcystic adenoma combined with an intraductal papillary mucinous tumor of the pancreas in a 69-year-old man. Abdominal computed tomography scans demonstrated an incidental cystic mass in the body with cystic dilatation of the duct in the head of the pancreas. Central pancreatectomy with pancreatico-jejunostomy, and cyst excision of the pancreatic head were performed. Histologic examination demonstrated a serous microcystic cystadenoma in the body coexisting with an intraductal papillary mucinous adenoma in the head of the pancreas. This case study highlights the importance of careful intra-operative and pathologic examination for synchronous pancreatic tumors.
Solitary Fibrous Tumor of the Liver: A Case Report.
Hee Chul Yu, Baik Hwan Cho, Young Kon Kim, Sang Jae Noh, Woo Sung Moon
Korean J Pathol. 2010;44(5):536-539.
DOI: https://doi.org/10.4132/KoreanJPathol.2010.44.5.536
  • 3,157 View
  • 21 Download
  • 1 Crossref
AbstractAbstract PDF
Solitary fibrous tumor is an uncommon neoplasm of mesenchymal origin that primarily affects the pleura. This tumor has been rarely found in liver parenchyma. We present an additional case of a solitary fibrous tumor in the liver of a 46-year-old woman. A contrast-enhanced magnetic resonance image revealed a well-defined round hepatic mass with strong homogeneous enhancement on arterial phase imaging. The tumor was composed of cytologically bland spindle cells with alternating hypercellular and hypocellular sclerotic areas. Immunohistochemistry indicated that the tumor cells were positive for vimentin, CD34, CD99 and smooth muscle actin, but negative for cytokeratin, human melanoma black 45, CD117, bcl-2, and S-100 protein.

Citations

Citations to this article as recorded by  
  • Meningeal Solitary Fibrous Tumors with Delayed Extracranial Metastasis
    Nayoung Han, Hannah Kim, Soo Kee Min, Sun-Ha Paek, Chul-Kee Park, Seung-Hong Choi, U-Ri Chae, Sung-Hye Park
    Journal of Pathology and Translational Medicine.2016; 50(2): 113.     CrossRef
Original Article
Expression and Prognostic Significance of Serum Response Factor in Cholangiocarcinoma.
Shin Young Park, Kyu Yun Jang, Yo Na Kim, Hee Jin Kim, Ho Sung Park, Myoung Ja Chung, Hee Chul Yu, Baik Hwan Cho, Kyoung Ryul Kim, Woo Sung Moon
Korean J Pathol. 2009;43(6):517-522.
DOI: https://doi.org/10.4132/KoreanJPathol.2009.43.6.517
  • 3,295 View
  • 18 Download
  • 2 Crossref
AbstractAbstract PDF
BACKGROUND
Serum response factor (SRF) is a transcriptional factor that plays an important role in cell growth and differentiation for several types of cells. The expression of SRF in cholangiocarcinoma (CC) and its potential role has not been examined. The aim of this study was to determine the relationship between the expression of SRF in CC and the clinicopathological parameters, as well as patient survival.
METHODS
We analyzed the expression of SRF in 84 surgically resected cases of CC (33 cases of intrahepatic CC [ICC] and 51 cases of extrahepatic CC [ECC]) by using immunohistochemistry. RESULTS: The positive expression of SRF was detected in 48.8% of the cases of CC (42.4% in ICC, 52.9% in ECC). SRF was predominantly expressed in the CC cells with intense labeling in the nucleus. A SRF expression was significantly associated with the cell proliferation rate (Ki-67 labeling index, p=0.046) and poor patient survival (p=0.002). The tumor differentiation (p=0.038), the T category (p<0.001), lymph node and distant metastasis (p<0.001, p=0.009) and nerve and vessel invasion (p=0.010, p=0.012) were also found to be significantly associated with a poor CC prognosis. CONCLUSIONS: These results suggest that the SRF may play a role in the tumor cell proliferation of CC, and its expression in tumor cells can provide additional prognostic information.

Citations

Citations to this article as recorded by  
  • Serum response factor induces epithelial to mesenchymal transition with resistance to sorafenib in hepatocellular carcinoma
    JUN SANG BAE, SANG JAE NOH, KYOUNG MIN KIM, KYU YUN JANG, MYOUNG JA CHUNG, DAE GOHN KIM, WOO SUNG MOON
    International Journal of Oncology.2014; 44(1): 129.     CrossRef
  • Clinicopathologic significance of serum response factor expression in colorectal adenocarcinomas
    Se Min Jang, Young Jin Jun, Hulin Han, Kang Hong Lee, Ki-Seok Jang, Seung Sam Paik
    Basic and Applied Pathology.2011; 4(2): 46.     CrossRef

J Pathol Transl Med : Journal of Pathology and Translational Medicine