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1.
J Low Genit Tract Dis ; 15(1): 6-10, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21192169

RESUMO

OBJECTIVE: Morphologic distinction between atypical glandular cells not otherwise specified (AGC-NOS) and AGC-favor neoplasia (AGC-FN) can be difficult. Distinction between these entities is important as the American Society for Colposcopy and Cervical Pathology 2006 consensus guidelines state that management of AGC-NOS differs from that of AGC-FN. The objective of this study was to determine the potential role of ProExC immunocytochemical triage of AGC-NOS. MATERIALS AND METHODS: Cytopathology records from a pathology practice were reviewed from January 2006 to December 2009 to identify AGC-NOS liquid-based Pap smears with subsequent biopsy correlation. Archival slides were examined, and ProExC immunocytochemistry was performed. The AGC groups were assessed for nuclear staining, and results were correlated with subsequent biopsy findings. RESULTS: Twenty-eight AGC-NOS cases with biopsy correlation were identified: 13 with subsequent high-grade neoplastic or malignant (positive) diagnoses and 15 with benign diagnoses. Of 13 AGC-NOS cases with positive diagnosis, 10 were ProExC-positive and 3 were ProExC-negative (metastatic tumors from distant sites). Of 15 AGC cases with benign follow-up, 13 were ProExC-negative and 2 were ProExC-positive (sensitivity, 77%; specificity, 87%). For patients with cervical intraepithelial neoplasia or carcinoma originating from the female genital tract, 100% (10/10) were ProExC-positive (sensitivity, 100%; specificity, 87%). CONCLUSIONS: Results suggest that ProExC-positive AGC-NOS may be classified as AGC-FN. Although positive immunocytochemical staining for ProExC requires management similar to AGC-FN, negative staining does not rule out malignancy such as metastatic tumor. Management for ProExC-negative AGC-NOS cases should proceed according to the current guidelines for AGC-NOS.


Assuntos
Antígenos de Neoplasias/análise , Proteínas de Ciclo Celular/análise , Colo do Útero/patologia , DNA Topoisomerases Tipo II/análise , Proteínas de Ligação a DNA/análise , Proteínas Nucleares/análise , Lesões Pré-Cancerosas/diagnóstico , Neoplasias do Colo do Útero/diagnóstico , Adulto , Idoso , Biópsia , Técnicas Citológicas/métodos , Feminino , Humanos , Imuno-Histoquímica/métodos , Pessoa de Meia-Idade , Componente 2 do Complexo de Manutenção de Minicromossomo , Lesões Pré-Cancerosas/patologia , Sensibilidade e Especificidade , Neoplasias do Colo do Útero/patologia
2.
Acta Cytol ; 53(5): 581-3, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19798888

RESUMO

BACKGROUND: Anaplastic thyroid carcinoma (ATC) is a highly aggressive, undifferentiated carcinoma that may arise on top of normal or abnormal thyroid. Making the diagnosis by fine needle aspiration (FNA) of the thyroid with a long-standing history of multinodular goiter (MNG) is not uncommon. We report a case discussing the cytopathologic findings and the relationship with long-standing goiter and thyroid exposure to radioactive iodine treatment. CASE: A 90-year-old male patient presented with a > 45-year history of MNG that was associated with thyrotoxicosis and multiple courses of radioiodine (I-131) treatment. He developed recent symptoms of dyspnea, dysphagia, neck welling and uniintentional weight loss. Computed tomography of the neck was done revealing a large MNG with retrosternal extension and calcifications. FNA was performed revealing highly anaplastic cells with a colloid background and presence of neutrophils. The diagnosis of ATC was made. The patient refused any kind of management and was discharged upon his request. He died 2 days after the procedure, and no autopsy was performed. CONCLUSION: ATC is an aggressive, undifferentiated thyroid carcinoma that can be diagnosed by FNA and save the patient a surgical intervention. A background of MNG and history of radioactive iodine therapy is not uncommon.


Assuntos
Biópsia por Agulha Fina , Carcinoma/patologia , Bócio Nodular/complicações , Radioisótopos do Iodo/efeitos adversos , Neoplasias Induzidas por Radiação/patologia , Neoplasias da Glândula Tireoide/patologia , Tireotoxicose/radioterapia , Idoso de 80 Anos ou mais , Carcinoma/etiologia , Evolução Fatal , Humanos , Imuno-Histoquímica , Masculino , Neoplasias Induzidas por Radiação/etiologia , Valor Preditivo dos Testes , Fatores de Risco , Neoplasias da Glândula Tireoide/etiologia , Tireotoxicose/etiologia , Tomografia Computadorizada por Raios X , Recusa do Paciente ao Tratamento
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