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1.
Histopathology ; 79(3): 416-426, 2021 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-33754384

RESUMO

AIMS: Appendiceal well-differentiated neuroendocrine tumours (NETs) are usually incidental and clinically benign. Several studies have reported different risk factors for nodal metastasis. The aim of this study was to investigate our appendiceal NETs (App-NETs) to determine the factors associated with malignant behaviour. METHODS AND RESULTS: For 120 App-NETs, we reviewed the clinical presentation and follow-up, including serum chromogranin A (CgA) levels, and compiled several microscopic variables. Pathological factors were compared with nodal status and time to biochemical recurrence (elevated serum CgA level) by the use of Cox regression. We also reviewed similar App-NET data in the Surveillance, Epidemiology, and End Results (SEER) Programme. Among our 120 cases, seven patients had positive lymph nodes, and nine developed subsequent elevation of CgA levels; none developed distant metastases or died of disease. Only three patients had grade 2 NETs; none had nodal disease, and one developed an elevated CgA level. Increasing tumour size was associated with an increased risk of nodal disease [odds ratio (OR) 4.99, P = 0.0055). All seven node-positive cases were ≥13 mm. Factors associated with elevated CgA levels included age (OR 1.04, P = 0.041), pT4 disease (OR 10.22, P = 0.033), and nodal disease (OR 24.0, P = 0.012), but not size (OR 2.13, P = 0.072). Of the 1492 reported App-NETs in the SEER database with data on tumour size, 137 (9%) were pN1; only five of these (4%) were coded as being <5 mm. CONCLUSIONS: Small (<5 mm) App-NETs that do not invade the serosa or mesoappendix appear to be overwhelmingly benign and low-grade, requiring neither Ki67 staining nor synoptic reporting. Given their indolent behaviour, different nomenclature or staging may be more appropriate for these NETs.


Assuntos
Neoplasias do Apêndice/patologia , Neoplasias Intestinais/patologia , Tumores Neuroendócrinos/patologia , Neoplasias Pancreáticas/patologia , Neoplasias Gástricas/patologia , Apendicectomia , Apêndice/patologia , Feminino , Humanos , Antígeno Ki-67/análise , Metástase Linfática/patologia , Masculino , Estadiamento de Neoplasias , Prognóstico , Fatores de Risco
2.
Diagn Cytopathol ; 49(7): E262-E268, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-33484239

RESUMO

Sclerosing mucoepidermoid carcinoma with eosinophilia (SMECE) is a rare malignancy in the thyroid: only 56 cases with histologic descriptions are reported in the literature and fewer reports describe the cytomorphology. Given the rarity of SMECE, data on the cytomorphologic and molecular features are limited. We report a case of a 53-year-old woman with a 5 cm left thyroid mass. Fine-needle aspiration (FNA) revealed atypia of undetermined significance and pathology of left thyroid lobectomy specimen showed SMECE. Additionally, a left pre-auricular lump was noted and FNA followed by left superficial parotidectomy showed basal cell adenoma. Next-generation sequencing showed point mutations in NTRK3 and NF1. Unlike salivary gland mucoepidermoid carcinoma, MAML2 translocations are not present in SMECE. Even though it is a rare entity, awareness of SMECE of the thyroid is important. In this case report we review the cytomorphologic, histologic, and molecular features.


Assuntos
Adenoma/patologia , Carcinoma Mucoepidermoide/patologia , Eosinofilia/patologia , Neoplasias Primárias Múltiplas/patologia , Neoplasias Parotídeas/patologia , Neoplasias da Glândula Tireoide/patologia , Adenoma/genética , Carcinoma Mucoepidermoide/genética , Feminino , Humanos , Pessoa de Meia-Idade , Neoplasias Primárias Múltiplas/genética , Neurofibromina 1/genética , Neoplasias Parotídeas/genética , Mutação Puntual , Receptor trkC/genética , Neoplasias da Glândula Tireoide/genética
3.
Hum Pathol ; 92: 101-106, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31430494

RESUMO

Appendiceal endometriosis, endosalpingiosis, and decidual lesions have received little attention in the pathology literature, meaning their clinicopathologic features remain unclear. We identified 72 cases of appendiceal gynecologic proliferations with available slides. Clinical presentation was recorded when available, and histologic findings were correlated with clinical data. Cases included conventional endometriosis (51), endosalpingiosis (14), and decidual lesions (7). The patients with endosalpingiosis were significantly older (median 45 years) than those with endometriosis (median 34 years, P = .0085) or decidual lesions (median 31 years, P = .0088). Most endometriosis patients presented with known/suspected endometriosis (20/51, 39%), while acute appendicitis was the most common presentation for patients with endosalpingiosis (5/14, 36%) or a decidual lesion (5/7, 71%). Few patients presenting with appendicitis were ever diagnosed with extra-appendiceal disease. All 51 endometriosis cases showed both glands and stroma, and 18 (35%) had hemosiderin. One case progressed to endometrioid adenocarcinoma. Endosalpingiosis was an incidental finding in all cases, confined to the serosa in 4 and extending intramurally in 10. Four of the 7 patients with a decidual lesion were pregnant, and 2 others were taking oral contraceptives. The cases included florid decidualized endometriosis (5) and deciduosis (2). Two cases spread transmurally and effectively obliterated the appendix. Conventional appendiceal endometriosis can have several clinical presentations. Patients with it who present with acute appendicitis rarely develop it elsewhere. Appendiceal endosalpingiosis is rare and effectively incidental. Decidualized endometriosis may overtake the entire appendix.


Assuntos
Apendicite/patologia , Apêndice/patologia , Carcinoma Endometrioide/patologia , Doenças do Ceco/patologia , Endometriose/patologia , Adolescente , Adulto , Idoso , Neoplasias do Apêndice/patologia , Proliferação de Células , Progressão da Doença , Feminino , Humanos , Pessoa de Meia-Idade , Adulto Jovem
4.
Am J Clin Pathol ; 151(1): 100-107, 2019 01 01.
Artigo em Inglês | MEDLINE | ID: mdl-30285068

RESUMO

Objectives: Indications for cholecystectomy have changed dramatically over the past three decades. Cystoisospora belli has been reported in cholecystectomy specimens of immunocompetent patients. The present study was designed to determine the prevalence and clinical association of C belli in the gallbladder. Methods: The study included retrospective review of cholecystectomy specimens (n = 401) removed for various indications, and a prospective cohort of cholecystectomy specimens (n = 22) entirely submitted for histologic evaluation. Correlations of presence of C belli with age, sex, clinical indication, and abnormalities of preoperative laboratory values were assessed by Fisher exact test. Results: C belli was identified in 39/401 (9.7%) of the retrospective cohort, and 6/22 (27.3%) of the entirely submitted specimens. The presence of C belli showed no correlation with age, sex, clinical indication, or laboratory abnormalities. Conclusions: C belli resides in a latent state in the gallbladder and may be best considered a commensal organism.


Assuntos
Coccídios/isolamento & purificação , Coccidiose/parasitologia , Doenças da Vesícula Biliar/parasitologia , Adolescente , Adulto , Colecistectomia , Coccidiose/epidemiologia , Coccidiose/patologia , Coccidiose/cirurgia , Estudos de Coortes , Feminino , Vesícula Biliar/parasitologia , Vesícula Biliar/patologia , Doenças da Vesícula Biliar/epidemiologia , Doenças da Vesícula Biliar/patologia , Doenças da Vesícula Biliar/cirurgia , Humanos , Masculino , Pessoa de Meia-Idade , Prevalência , Estudos Prospectivos , Estudos Retrospectivos , Adulto Jovem
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