2020
DOI: 10.1007/s12029-020-00500-1
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Clinicopathological Features of Two Extremely Rare Hepatocellular Carcinoma Variants: a Brief Review of Fibrolamellar and Scirrhous Hepatocellular Carcinoma

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Cited by 7 publications
(16 citation statements)
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“…After these macroscopic definitions and macroscopic heterogeneity, it is necessary to mention microscopic heterogeneity. This heterogeneity is also reflected in the histopathological subtyping of HCC [71]. In the 5th edition of WHO classification of the tumors of the digestive system (2019), the subtypes of HCC are as follows; fibrolamellar, scirrhus, cear cell type, steatohepatitic, macrotrabecular massive, chromophobe, neutrophil-rich, lympocyte-rich [1].…”
Section: Pathological Featuresmentioning
confidence: 99%
“…After these macroscopic definitions and macroscopic heterogeneity, it is necessary to mention microscopic heterogeneity. This heterogeneity is also reflected in the histopathological subtyping of HCC [71]. In the 5th edition of WHO classification of the tumors of the digestive system (2019), the subtypes of HCC are as follows; fibrolamellar, scirrhus, cear cell type, steatohepatitic, macrotrabecular massive, chromophobe, neutrophil-rich, lympocyte-rich [1].…”
Section: Pathological Featuresmentioning
confidence: 99%
“…4,5,[23][24][25] Grossly, S-HCC often appears as a multilobulated solid subcapsular mass that has a firm consistency due to the intratumoral fibrous content and thus appears somewhat similar to an iCCA on gross examination. [24][25][26] Tumor necrosis or hemorrhage is less frequent in S-HCC compared with conventional HCCs. 24,27 At low-power magnification, the tumor cells of S-HCCs form nests or trabeculae that appear embedded within a dense collagenous stroma.…”
Section: Scirrhous Hccmentioning
confidence: 99%
“…33 It is important that S-HCC is not to be confused for FLHCC, another subtype of HCC that also contains abundant intratumoral fibrous stroma. 26 Fibrolamellar HCC, which is more common in Western countries and very rare in Asia, shows unique clinical, histomorphological, and molecular characteristics. Clinically, it is mostly diagnosed in adolescents and young adults without underlying chronic liver disease and without the typical risk factors for HCC.…”
Section: Scirrhous Hccmentioning
confidence: 99%
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“…It is characterized by a central scar that could appear as a central area of hyperechogenicity. The next diagnostic step is frequently the computerized tomography (CT) study, in which FLHCC is shown as a lobulated lesion with good edge definition and a central scar with calcification nodules [ 5 ]. The enhancement is heterogeneous due to different portions of cellular and fibrous tissue.…”
Section: Introductionmentioning
confidence: 99%