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Myoepithelioma, myoepithelioma-like, and chondroid soft-tissue tumors arising at acral sites: a review

Human pathology, 2023-10, Vol.140, p.66-74

2023

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What is new in pericytomatous, myoid, and myofibroblastic tumors?

Virchows Archiv : an international journal of pathology, 2020, Vol.476 (1), p.57-64

2020

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Clinical, Endoscopic, and Histologic Findings Distinguish Eosinophilic Esophagitis From Gastroesophageal Reflux Disease

Clinical gastroenterology and hepatology, 2009-12, Vol.7 (12), p.1305-1313

2009

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Mesenchymal chondrosarcomas showing immunohistochemical evidence of rhabdomyoblastic differentiation: a potential diagnostic pitfall

Human pathology, 2018-07, Vol.77, p.28-34

2018

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Novel PPP1CB‐ALK fusion in spindle cell tumor defined by S100 and CD34 coexpression and distinctive stromal and perivascular hyalinization

Genes chromosomes & cancer, 2020-08, Vol.59 (8), p.495-499

2020

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Intraosseous glomus tumours with NOTCH2/3 fusions: two cases presenting in the long bones with review of the literature

Histopathology, 2024-10, Vol.85 (4), p.690-693

2024

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Clinical and endoscopic characteristics do not reliably differentiate PPI-responsive esophageal eosinophilia and eosinophilic esophagitis in patients undergoing upper endoscopy: a prospective cohort study

The American journal of gastroenterology, 2013-12, Vol.108 (12), p.1854-1860

2013

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Updates in spindle cell/pleomorphic lipomas

Seminars in diagnostic pathology, 2019-03, Vol.36 (2), p.105-111

2019

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Fusion gene profile of biphenotypic sinonasal sarcoma: an analysis of 44 cases

Histopathology, 2016-12, Vol.69 (6), p.930-936

2016

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Morphologic Spectrum of Desmoid-Type Fibromatosis

American journal of clinical pathology, 2016-03, Vol.145 (3), p.332-340

2016

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Perinephric myxoid pseudotumor of fat: a distinctive pseudoneoplasm most often associated with non-neoplastic renal disease

Human pathology, 2019-05, Vol.87, p.37-43

2019

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Esophageal dilation in eosinophilic esophagitis: safety and predictors of clinical response and complications

Gastrointestinal endoscopy, 2010-04, Vol.71 (4), p.706-712

2010

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Infantile Sinonasal Myxoma Is Clinically and Genetically Distinct From Other Myxomas of the Craniofacial Bones and From Desmoid Fibromatosis

The American journal of surgical pathology, 2023-11, Vol.47 (11), p.1301-1315

2023

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Clear Cell Stromal Tumor of Lung: A Clinicopathologic, Immunohistochemical, and Molecular Characterization of 8 Cases

Modern pathology, 2024-10, p.100632, Article 100632

2024

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CD34-negative Solitary Fibrous Tumor: A Clinicopathologic Study of 25 Cases and Comparison With Their CD34-positive Counterparts

The American journal of surgical pathology, 2021-12, Vol.45 (12), p.1616-1625

2021

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Diagnostic Utility of IDH1/2 Mutations to Distinguish Dedifferentiated Chondrosarcoma from Undifferentiated Pleomorphic Sarcoma of Bone

Human pathology, 2017-07, Vol.65, p.239-246

2017

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ALK‐rearranged, CD34‐positive spindle cell neoplasms resembling dermatofibrosarcoma protuberans: a study of seven cases

Histopathology, 2024-10, Vol.85 (4), p.649-659

2024

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The utility of DNA methylation profiling in the diagnosis of un-, de- and trans-differentiated melanoma: a series of 11 cases

Histopathology, 2024-09

2024

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EWSR1::ATF1 fusions characterize a group of extra-abdominal epithelioid and round cell mesenchymal neoplasms, phenotypically overlapping with sclerosing epithelioid fibrosarcomas, and intra-abdominal FET::CREB fusion neoplasms

Virchows Archiv : an international journal of pathology, 2024-07

2024

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Histiocyte-rich rhabdomyoblastic tumor: rhabdomyosarcoma, rhabdomyoma, or rhabdomyoblastic tumor of uncertain malignant potential? A histologically distinctive rhabdomyoblastic tumor in search of a place in the classification of skeletal muscle neoplasms

Modern pathology, 2019-03, Vol.32 (3), p.446-457

2019

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Chondroblastomas presenting in adulthood: a study of 39 patients with emphasis on histological features and skeletal distribution

Histopathology, 2020-01, Vol.76 (2), p.308-317

2020

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DNA Methylation Profiling Distinguishes Adamantinoma-Like Ewing Sarcoma From Conventional Ewing Sarcoma

Modern pathology, 2023-11, Vol.36 (11), p.100301-100301, Article 100301

2023

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Fibrous hamartoma of infancy: a clinicopathologic study of 145 cases, including 2 with sarcomatous features

Modern pathology, 2017-04, Vol.30 (4), p.474-485

2017

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Myxofibrosarcoma in Adolescents and Young Adults: A Clinicopathologic Study of 17 Cases

Human pathology, 2023-12, Vol.142, p.90-95

2023

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ERG expression in chondrogenic bone and soft tissue tumours

Journal of clinical pathology, 2015-02, Vol.68 (2), p.125-129

2015

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Myoepithelioma, myoepithelioma-like, and chondroid soft-tissue tumors arising at acral sites: a review

What is new in pericytomatous, myoid, and myofibroblastic tumors?

Clinical, Endoscopic, and Histologic Findings Distinguish Eosinophilic Esophagitis From Gastroesophageal Reflux Disease

Mesenchymal chondrosarcomas showing immunohistochemical evidence of rhabdomyoblastic differentiation: a potential diagnostic pitfall

Novel PPP1CB‐ALK fusion in spindle cell tumor defined by S100 and CD34 coexpression and distinctive stromal and perivascular hyalinization

Intraosseous glomus tumours with NOTCH2/3 fusions: two cases presenting in the long bones with review of the literature

Clinical and endoscopic characteristics do not reliably differentiate PPI-responsive esophageal eosinophilia and eosinophilic esophagitis in patients undergoing upper endoscopy: a prospective cohort study

Updates in spindle cell/pleomorphic lipomas

Fusion gene profile of biphenotypic sinonasal sarcoma: an analysis of 44 cases

Morphologic Spectrum of Desmoid-Type Fibromatosis

Perinephric myxoid pseudotumor of fat: a distinctive pseudoneoplasm most often associated with non-neoplastic renal disease

Esophageal dilation in eosinophilic esophagitis: safety and predictors of clinical response and complications

Infantile Sinonasal Myxoma Is Clinically and Genetically Distinct From Other Myxomas of the Craniofacial Bones and From Desmoid Fibromatosis

Clear Cell Stromal Tumor of Lung: A Clinicopathologic, Immunohistochemical, and Molecular Characterization of 8 Cases

CD34-negative Solitary Fibrous Tumor: A Clinicopathologic Study of 25 Cases and Comparison With Their CD34-positive Counterparts

Diagnostic Utility of IDH1/2 Mutations to Distinguish Dedifferentiated Chondrosarcoma from Undifferentiated Pleomorphic Sarcoma of Bone

ALK‐rearranged, CD34‐positive spindle cell neoplasms resembling dermatofibrosarcoma protuberans: a study of seven cases

The utility of DNA methylation profiling in the diagnosis of un-, de- and trans-differentiated melanoma: a series of 11 cases

EWSR1::ATF1 fusions characterize a group of extra-abdominal epithelioid and round cell mesenchymal neoplasms, phenotypically overlapping with sclerosing epithelioid fibrosarcomas, and intra-abdominal FET::CREB fusion neoplasms

Histiocyte-rich rhabdomyoblastic tumor: rhabdomyosarcoma, rhabdomyoma, or rhabdomyoblastic tumor of uncertain malignant potential? A histologically distinctive rhabdomyoblastic tumor in search of a place in the classification of skeletal muscle neoplasms

Chondroblastomas presenting in adulthood: a study of 39 patients with emphasis on histological features and skeletal distribution

DNA Methylation Profiling Distinguishes Adamantinoma-Like Ewing Sarcoma From Conventional Ewing Sarcoma

Fibrous hamartoma of infancy: a clinicopathologic study of 145 cases, including 2 with sarcomatous features

Myxofibrosarcoma in Adolescents and Young Adults: A Clinicopathologic Study of 17 Cases

ERG expression in chondrogenic bone and soft tissue tumours

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