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2.
Am J Clin Pathol ; 154(3): 353-361, 2020 08 05.
Artigo em Inglês | MEDLINE | ID: mdl-32525520

RESUMO

OBJECTIVES: Superficial pleomorphic liposarcoma (PL) has a favorable prognosis compared to deeply seated PL. Given developments in the classification of lipomatous neoplasms, we reappraised a series of cases. METHODS: Retrospective clinicopathologic evaluation and genome-wide single-nucleotide polymorphism (SNP) microarray studies were performed for cases previously designated superficial PL. RESULTS: Four cases were identified (age, 48-70 years). Two were dermally confined, whereas two were superficial subcutaneous; no recurrences or metastases were reported. Tumors demonstrated pleomorphic spindled morphology with variable cellularity. Multivacuolated atypical lipoblasts were focal in 3 and abundant in 1. Dermal tumors demonstrated atypical cells within sclerotic collagen. Genome-wide SNP microarray studies revealed consistent gains and losses, including losses at the 13q14.2 locus encompassing RB1 and DLEU2 and deletion/disruption of the TP53 locus. Although subcutaneous examples showed genomic changes similar to deep PL, the dermal examples showed fewer genetic alterations, including changes reported in the spectrum of atypical spindle cell/pleomorphic lipomatous tumors (ASPLT). All lacked MDM2 amplification. CONCLUSIONS: Careful integration of histologic and genetic features may improve classification of lipomatous neoplasms with atypia, allowing reclassification of some superficial PL as ASPLT.


Assuntos
Lipossarcoma/patologia , Mutação , Polimorfismo de Nucleotídeo Único , Neoplasias de Tecidos Moles/patologia , Idoso , Biomarcadores Tumorais/genética , Feminino , Estudo de Associação Genômica Ampla , Humanos , Lipossarcoma/genética , Masculino , Pessoa de Meia-Idade , Neoplasias de Tecidos Moles/genética
3.
Hum Pathol ; 104: 9-17, 2020 10.
Artigo em Inglês | MEDLINE | ID: mdl-32681945

RESUMO

Peyronie disease (PD) is a benign, superficial fibromatosis involving the fascial structures of the penis, causing deformity, pain, and loss of function, for which there are few contemporary studies of the histopathology. We performed a multi-institutional review of 74 routine and consultation specimens submitted with clinical concern for PD. Of these, three non-PD lesions were identified and excluded (a myointimoma, a mammary-type myofibroblastoma, and fibrocalcific atherosclerosis). Of the 71 confirmed to be PD, the majority of patients were white (83%), with a median age of 55 years (range: 26-88). The dorsal aspect of the penis was the most common site involved (78%), followed by lateral (12%) and ventral (10%) aspects. The median degree of curvature was 70° (range: 20-360°). On review, three overall histologic patterns characterized the lesions resected: dense fibrotic plaque (61%), dense fibrotic plaque with focal or patchy metaplastic ossification (35%), and plaque composed predominantly of metaplastic ossification (4%). The fibrotic component was predominantly nodular (18%), hyalinized/lamellar (46%), or mixed (32%), excepting two cases consisting entirely of metaplastic bone. Chronic inflammation, when present, was most often focal and perivascular in distribution. In one case, an excision after collagenase treatment showed myxoid change and increased stromal cellularity. Overall, these findings define the range of PD histology, particularly emphasizing that the calcification noted clinically nearly always represents bona fide metaplastic ossification. Such context will be of value in evaluating specimens prospectively, in light of changing practices and the use of new technologies for treatment.


Assuntos
Ossificação Heterotópica/patologia , Induração Peniana/patologia , Pênis/patologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Bases de Dados Factuais , Fibrose , Humanos , Masculino , Metaplasia , Pessoa de Meia-Idade , Ossificação Heterotópica/epidemiologia , Induração Peniana/epidemiologia , Prevalência , Estudos Retrospectivos , Estados Unidos
4.
Surg Pathol Clin ; 11(4): 837-876, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30447845

RESUMO

Mesenchymal neoplasms of the genitourinary (GU) tract often pose considerable diagnostic challenges due to their wide morphologic spectrum, relative rarity, and unexpected incidence at GU sites. Soft tissue tumors arise throughout the GU tract, whether from adventitia surrounding or connective tissues within the kidneys, urinary bladder, and male and female genital organs. This selected article focuses on a subset of these lesions, ranging from benign to malignant and encompassing a range of patterns of mesenchymal differentiation, where recent scholarship has lent greater insight into their clinical, molecular, or diagnostic features.


Assuntos
Mesenquimoma/patologia , Neoplasias de Tecido Conjuntivo e de Tecidos Moles/patologia , Neoplasias Urogenitais/patologia , Diagnóstico Diferencial , Humanos , Mesenquimoma/diagnóstico , Mesenquimoma/genética , Neoplasias de Tecido Conjuntivo e de Tecidos Moles/diagnóstico , Neoplasias de Tecido Conjuntivo e de Tecidos Moles/genética , Neoplasias Urogenitais/diagnóstico , Neoplasias Urogenitais/genética
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