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The American Journal of Surgical Pathology, ISSN 0147-5185, 02/2014, Volume 38, Issue 2, pp. 176 - 188
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 09/2015, Volume 39, Issue 9, pp. 1181 - 1196
An increasing number of TFE3 rearrangement–associated tumors, such as TFE3 rearrangement–associated perivascular epithelioid cell tumors (PEComas), melanotic... 
Translocation | PSF/SFPQ | Molecular genetics | Melanotic Xp11 translocation renal cancer | TFE3 | FISH | Perivascular epithelioid cell tumor | Rearrangement | molecular genetics | SURGERY | DIAGNOSIS | perivascular epithelioid cell tumor | PSF | translocation | URINARY-BLADDER | IN-SITU-HYBRIDIZATION | PATHOLOGY | SOFT-TISSUE | BREAK-APART FISH | NEOPLASM PECOMA | FEATURES | melanotic Xp11 translocation renal cancer | SFPQ | OF-THE-LITERATURE | CARCINOMA | rearrangement | MORPHOLOGY | Immunohistochemistry | Predictive Value of Tests | RNA-Binding Proteins - genetics | Translocation, Genetic | Kidney Neoplasms - genetics | Prognosis | Mitosis | Humans | Middle Aged | Kidney Neoplasms - classification | Male | Kidney Neoplasms - chemistry | Chromosomes, Human, X | Molecular Diagnostic Techniques | Time Factors | Melanoma - genetics | Adult | Female | Melanoma - classification | Child | Perivascular Epithelioid Cell Neoplasms - chemistry | Perivascular Epithelioid Cell Neoplasms - classification | Melanoma - chemistry | Genetic Predisposition to Disease | Biomarkers, Tumor - analysis | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - analysis | Gene Fusion | In Situ Hybridization, Fluorescence | Melanoma - pathology | Kidney Neoplasms - mortality | Reverse Transcriptase Polymerase Chain Reaction | PTB-Associated Splicing Factor | Perivascular Epithelioid Cell Neoplasms - pathology | Phenotype | Perivascular Epithelioid Cell Neoplasms - genetics | Gene Rearrangement | Adolescent | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics | Kidney Neoplasms - pathology | Aged | Biomarkers, Tumor - genetics | Melanoma - mortality | Perivascular Epithelioid Cell Neoplasms - mortality | Index Medicus
Journal Article
Neuro-Oncology, ISSN 1522-8517, 06/2013, Volume 15, Issue 6, pp. 727 - 734
Journal Article
Surgical Case Reports, ISSN 2198-7793, 12/2016, Volume 2, Issue 1, pp. 1 - 7
Angiomyolipoma (AML) arising in the liver is rare and usually benign, but it occasionally has malignant potential. A 58-year-old man with a liver tumor... 
Perivascular epithelioid cell | Malignant potential | Hepatic angiomyolipoma | Medicine & Public Health | Surgery
Journal Article
Archives of Pathology and Laboratory Medicine, ISSN 0003-9985, 03/2017, Volume 141, Issue 3, pp. 463 - 469
Journal Article
Surgical Pathology Clinics, ISSN 1875-9181, 06/2016, Volume 9, Issue 2, pp. 269 - 287
This review covers gynecologic manifestations that may occur in rare hereditary syndromes. Recent advances in disorders, such as hereditary leiomyomatosis,... 
Cowden syndrome | Maffucci syndrome | Hereditary leiomyomatosis renal cell carcinoma syndrome | Tuberous sclerosis | Von Hippel-Lindau | Ollier disease | Carney complex | Nevoid basal cell carcinoma syndrome | Neoplastic Syndromes, Hereditary - pathology | Prognosis | Uterine Neoplasms - pathology | Humans | Lymphangioleiomyomatosis - pathology | Carney Complex - pathology | von Hippel-Lindau Disease - diagnosis | Genital Neoplasms, Female - diagnosis | Tuberous Sclerosis - pathology | Basal Cell Nevus Syndrome - pathology | von Hippel-Lindau Disease - pathology | Leiomyomatosis - diagnosis | Skin Neoplasms - diagnosis | Carney Complex - genetics | Leiomyomatosis - pathology | Female | Neoplastic Syndromes, Hereditary - genetics | Tuberous Sclerosis - diagnosis | Uterine Neoplasms - diagnosis | Carney Complex - diagnosis | Genital Neoplasms, Female - genetics | Skin Neoplasms - pathology | Uterine Neoplasms - genetics | Diagnosis, Differential | Hamartoma Syndrome, Multiple - genetics | Hamartoma Syndrome, Multiple - pathology | Basal Cell Nevus Syndrome - diagnosis | Neoplastic Syndromes, Hereditary - diagnosis | von Hippel-Lindau Disease - genetics | Enchondromatosis - diagnosis | Tuberous Sclerosis - genetics | Perivascular Epithelioid Cell Neoplasms - pathology | Hamartoma Syndrome, Multiple - diagnosis | Perivascular Epithelioid Cell Neoplasms - genetics | Skin Neoplasms - genetics | Basal Cell Nevus Syndrome - genetics | Enchondromatosis - pathology | Leiomyomatosis - genetics | Perivascular Epithelioid Cell Neoplasms - diagnosis | Genital Neoplasms, Female - pathology | Enchondromatosis - genetics | Lymphangioleiomyomatosis - diagnosis | Lymphangioleiomyomatosis - genetics
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