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“Oncocytoid Renal Cell Carcinomas After Neuroblastoma” Represent TSC-mutated Eosinophilic Solid and Cystic Renal Cell Carcinomas: Association With Prior Childhood Malignancy and Multifocality With Therapeutic Implications
“Oncocytoid Renal Cell Carcinomas After Neuroblastoma” Represent TSC-mutated Eosinophilic Solid and Cystic Renal Cell Carcinomas: Association With Prior Childhood Malignancy and Multifocality With Therapeutic Implications
The concept of oncocytoid renal cell carcinoma in patients who have survived neuroblastoma as a dist
Non-Neoplastic Thoracic Cysts: A Clinicopathologic Study of 136 Cases
Non-Neoplastic Thoracic Cysts: A Clinicopathologic Study of 136 Cases
Benign cysts of the thoracic cavity represent a group of rare lesions, the spectrum of which is expa
Incidence and Clinicopathologic Characteristics of Human Papillomavirus–independent Invasive Squamous Cell Carcinomas of the Cervix: A Morphologic, Immunohistochemical, and Human Papilloma-Virologic Study of 670 Cases
Incidence and Clinicopathologic Characteristics of Human Papillomavirus–independent Invasive Squamous Cell Carcinomas of the Cervix: A Morphologic, Immunohistochemical, and Human Papilloma-Virologic Study of 670 Cases
We aimed to determine the frequency of human papillomavirus–independent (HPVI) cervical squamous cel
PRAME Expression Is a Useful Tool in the Diagnosis of Primary and Metastatic Dedifferentiated and Undifferentiated Melanoma
PRAME Expression Is a Useful Tool in the Diagnosis of Primary and Metastatic Dedifferentiated and Undifferentiated Melanoma
Although mostly recognized in the metastatic setting dedifferentiated and undifferentiated melanomas
Subcutaneous Leiomyosarcoma: An Aggressive Malignancy Portending a Significant Risk of Metastasis and Death
Subcutaneous Leiomyosarcoma: An Aggressive Malignancy Portending a Significant Risk of Metastasis and Death
Subcutaneous leiomyosarcoma (LMS) is a rare, poorly understood variant. The current literature on th
A Novel Type of IDH-wildtype Glioma Characterized by Gliomatosis Cerebri-like Growth Pattern, TERT Promoter Mutation, and Distinct Epigenetic Profile
A Novel Type of IDH-wildtype Glioma Characterized by Gliomatosis Cerebri-like Growth Pattern, TERT Promoter Mutation, and Distinct Epigenetic Profile
Diffuse gliomas in adults encompass a heterogenous group of central nervous system neoplasms. In rec
Spiradenoma With Adenoid Cystic Carcinoma–like Changes: A Case Series of This Rare Variant With a Potential Diagnostic Pitfall
Spiradenoma With Adenoid Cystic Carcinoma–like Changes: A Case Series of This Rare Variant With a Potential Diagnostic Pitfall
Spiradenomas are benign cutaneous adnexal neoplasms with sweat gland differentiation that can manife
IRF8 in Conjunction With CD123 and CD20 to Distinguish Lupus Erythematosus Panniculitis From Subcutaneous Panniculitis-like T-Cell Lymphoma
IRF8 in Conjunction With CD123 and CD20 to Distinguish Lupus Erythematosus Panniculitis From Subcutaneous Panniculitis-like T-Cell Lymphoma
Distinguishing lupus erythematosus panniculitis (LEP) from subcutaneous panniculitis-like T-cell lym
The Spectrum of HPV-independent Penile Intraepithelial Neoplasia: A Proposal for Subclassification
The Spectrum of HPV-independent Penile Intraepithelial Neoplasia: A Proposal for Subclassification
Compared with vulva, precursor lesions of human papillomavirus (HPV)-independent invasive squamous c
Clinical, Morphologic, and Molecular Features of Benign and Intermediate-grade Melanocytic Tumors With Activating Mutations in MAP2K1
Clinical, Morphologic, and Molecular Features of Benign and Intermediate-grade Melanocytic Tumors With Activating Mutations in MAP2K1
Activating mutations in MAP2K1 can be seen in benign and intermediate-grade melanocytic neoplasms wi
Clinicopathologic Analysis and Molecular Profiling of Ovarian Steroid Cell Tumors
Clinicopathologic Analysis and Molecular Profiling of Ovarian Steroid Cell Tumors
Ovarian steroid and Leydig cell tumors (SCT and LCT, respectively) are rare stromal tumors, with agg
Germline APC Alterations May Predispose to Testicular Sex Cord-Stromal Tumors
Germline APC Alterations May Predispose to Testicular Sex Cord-Stromal Tumors
Sertoli cell tumor is a type of testicular sex cord-stromal tumor (TSCST) typically driven by gain-o
Unusual Aspects of Small Cell Carcinoma of the Ovary of Hypercalcaemic Type: Retained SMARCA4 Immunohistochemical Staining and Positive Staining With TLE1
Unusual Aspects of Small Cell Carcinoma of the Ovary of Hypercalcaemic Type: Retained SMARCA4 Immunohistochemical Staining and Positive Staining With TLE1
Small cell carcinoma of the ovary of hypercalcaemic type (SCCOHT) is a rare and aggressive ovarian n
Adamantinoma-like Ewing Sarcoma (ALES) May Harbor FUS Rearrangements: A Potential Diagnostic Pitfall
Adamantinoma-like Ewing Sarcoma (ALES) May Harbor FUS Rearrangements: A Potential Diagnostic Pitfall
Adamantinoma-like Ewing sarcoma (ALES) is a rare malignancy currently considered a variant of Ewing
sTRBC1 and cyTRBC1 Expression Distinguishes Indolent T-Lymphoblastic Proliferations From T-Lymphoblastic Leukemia/Lymphoma
sTRBC1 and cyTRBC1 Expression Distinguishes Indolent T-Lymphoblastic Proliferations From T-Lymphoblastic Leukemia/Lymphoma
Indolent T-lymphoblastic proliferation (iT-LBP) consists of a proliferation of non-neoplastic TdT+ T
Adenoid Ameloblastoma Shares Clinicopathologic, Immunohistochemical, and Molecular Features With Dentinogenic Ghost Cell Tumor: A Comparative Analysis
Adenoid Ameloblastoma Shares Clinicopathologic, Immunohistochemical, and Molecular Features With Dentinogenic Ghost Cell Tumor: A Comparative Analysis
The updated classification of odontogenic tumors by the World Health Organization (WHO) has included
PEComa of the Adrenal Gland: A Clinicopathologic Series of 7 Cases
PEComa of the Adrenal Gland: A Clinicopathologic Series of 7 Cases
PEComas are a family of mesenchymal neoplasms composed of histologically distinctive perivascular ep
Solitary Fibrous Tumor of the Pancreas: Analysis of 9 Cases With Literature Review
Solitary Fibrous Tumor of the Pancreas: Analysis of 9 Cases With Literature Review
Solitary fibrous tumor (SFT) has been increasingly reported in various anatomic sites. However, it i
Endometrial/Endometrioid Stromal Tumors With Extensive Whorling and CTNNB1 Translocation: A Report of 3 Cases
Endometrial/Endometrioid Stromal Tumors With Extensive Whorling and CTNNB1 Translocation: A Report of 3 Cases
Endometrial/endometrioid stromal tumors are rare and morphologically heterogenous, and their diagnos
CTNNB1 and APC Mutations in Sinonasal Myxoma: Expanding the Spectrum of Tumors Driven By WNT/β-catenin Pathway
CTNNB1 and APC Mutations in Sinonasal Myxoma: Expanding the Spectrum of Tumors Driven By WNT/β-catenin Pathway
Sinonasal myxoma (SNM) is a rare, benign mesenchymal neoplasm with distinct clinicopathologic featur
Clinicopathological Impacts of Expression of Neuronal Markers in Lymphangioleiomyomatosis
Clinicopathological Impacts of Expression of Neuronal Markers in Lymphangioleiomyomatosis
Lymphangioleiomyomatosis (LAM) is a tuberous sclerosis complex (TSC)-associated tumor, characterized
Genomic Analysis in the Categorization of Poorly Differentiated Primary Liver Carcinomas
Genomic Analysis in the Categorization of Poorly Differentiated Primary Liver Carcinomas
A subset of primary liver carcinomas (PLCs) cannot be classified as hepatocellular carcinoma (HCC) o
Positive GPNMB Immunostaining Differentiates Renal Cell Carcinoma With Fibromyomatous Stroma Associated With TSC1/2/MTOR Alterations From Others
Positive GPNMB Immunostaining Differentiates Renal Cell Carcinoma With Fibromyomatous Stroma Associated With TSC1/2/MTOR Alterations From Others
Renal cell carcinoma with fibromyomatous stroma (RCCFMS) include ELOC/TCEB1-mutated renal cell carci
Infantile Sinonasal Myxoma Is Clinically and Genetically Distinct From Other Myxomas of the Craniofacial Bones and From Desmoid Fibromatosis
Infantile Sinonasal Myxoma Is Clinically and Genetically Distinct From Other Myxomas of the Craniofacial Bones and From Desmoid Fibromatosis
Sinonasal myxomas are rare benign tumors of the maxillary bone and sinus. There is published evidenc
Comprehensive Clinical-Pathologic Assessment of Malignant Phyllodes Tumors: Proposing Refined Diagnostic Criteria
Comprehensive Clinical-Pathologic Assessment of Malignant Phyllodes Tumors: Proposing Refined Diagnostic Criteria
The latest World Health Organization classification of breast tumors recommends diagnosing malignant
Critical Appraisal of Histologic Grading for Mucoepidermoid Carcinoma of Salivary Gland: Is an Objective Prognostic 2-tiered Grading System Possible?
Critical Appraisal of Histologic Grading for Mucoepidermoid Carcinoma of Salivary Gland: Is an Objective Prognostic 2-tiered Grading System Possible?
Multiple 3-tiered grading systems exist for mucoepidermoid carcinoma (MEC), leading to controversial
Richard L. Kempson, MD, RIP
Richard L. Kempson, MD, RIP
Lauren V. Ackerman Laboratory of Surgical Pathology Washington University Medical Center St. Louis, MO Confli...
Reply: Salivary Gland Secretory Carcinoma: Clinicopathologic and Genetic Characteristics of 215 Cases and Proposal for a Grading System
Reply: Salivary Gland Secretory Carcinoma: Clinicopathologic and Genetic Characteristics of 215 Cases and Proposal for a Grading System
*Department of Pathology, Charles University, Faculty of Medicine †Bioptic Laboratory, Ltd ‡Information...
Clinical and Histopathologic Analyses of Nasopharyngeal Hyalinizing Clear Cell Carcinoma: A Series of 26 Cases With Molecular Confirmation
Clinical and Histopathologic Analyses of Nasopharyngeal Hyalinizing Clear Cell Carcinoma: A Series of 26 Cases With Molecular Confirmation
The aim of this study was to evaluate the clinicopathologic features, molecular characteristics, tre
Palisading Adenocarcinoma: A Morphologically Unique Salivary Gland Tumor With a Neuroendocrine-like Appearance and a Predilection for the Sublingual Glands of Women
Palisading Adenocarcinoma: A Morphologically Unique Salivary Gland Tumor With a Neuroendocrine-like Appearance and a Predilection for the Sublingual Glands of Women
Adenocarcinoma, not otherwise specified (NOS) is a heterogenous group of salivary gland tumors that
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