keyword
Keywords Immunohistochemical work up fo...

Immunohistochemical work up for hepatic metastatic tumors

https://read.qxmd.com/read/37547028/solid-tubulocystic-carcinoma-a-new-variant-of-intrahepatic-cholangiocarcinoma
#1
REVIEW
Iván A González, Wenyi Luo, Xuchen Zhang
A new variant of intrahepatic cholangiocarcinoma (iCCA) has been recognized in recent years presenting predominantly as a large hepatic mass in young woman with the characteristic expression of inhibin by immunohistochemistry. This variant iCCA was originally termed as cholangioblastic variant of iCCA, and subsequently proposed to be renamed as inhibin-positive hepatic carcinoma or solid-tubulocystic variant of iCCA to better reflect its immunohistochemical profile or morphologic spectrum. The tumor histologically is composed of small to medium sized cells with scant to moderate amount of eosinophilic cytoplasm heterogeneously organized in solid, tubular, and cystic growth patterns...
July 27, 2023: World Journal of Hepatology
https://read.qxmd.com/read/35681273/molecular-deciphering-of-primary-liver-neuroendocrine-neoplasms-confirms-their-distinct-existence-with-foregut-like-profile
#2
JOURNAL ARTICLE
Louis de Mestier, Rémy Nicolle, Nicolas Poté, Vinciane Rebours, François Cauchy, Olivia Hentic, Frédérique Maire, Maxime Ronot, Rachida Lebtahi, Alain Sauvanet, Valérie Paradis, Philippe Ruszniewski, Anne Couvelard, Jérôme Cros
Isolated hepatic localizations of neuroendocrine tumors (NETs) are generally considered as metastatic NETs of unknown primary but could correspond to primary hepatic NETs (PHNETs), a poorly explored entity. We aimed to describe the clinicopathological and molecular features of PHNETs and compare them with other primary NETs. We assembled a retrospective cohort of patients managed for hepatic localization of NET without extra-hepatic primary tumor after exhaustive clinical, imaging, and immunohistochemical characterization...
September 2022: Journal of Pathology
https://read.qxmd.com/read/25114821/malignant-mesenteric-perivascular-epithelioid-cell-neoplasm-presenting-as-an-intra-abdominal-fistula-in-a-49-year-old-female
#3
JOURNAL ARTICLE
Sakshi Kapur, Napoleon K Patel, Miles B Levin, Richard Huang
Perivascular epithelioid cell tumors are rare mesenchymal tumors arising from histologically and immunohistochemically distinctive perivascular epithelioid cells that express both myogenic and melanocytic markers. These tumors are known to arise from different organs in the body and usually have an unpredictable clinical course. We report a case of a 49-year-old female who presented with diffuse abdominal pain, fever, chills, and nonbilious vomiting for a day. Work-up revealed a mesenteric mass measuring 13...
2014: Case Reports in Oncological Medicine
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