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1.
AJR Am J Roentgenol ; 196(4): 795-800, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21427327

RESUMO

OBJECTIVE: PET cannot distinguish between bronchogenic carcinoma and granuloma, but positive scans may prompt surgery. We systematically evaluated the CT appearance of resected carcinomas and granulomas to identify features that could be used to reduce granuloma resections. MATERIALS AND METHODS: We retrospectively identified 93 consecutive patients between January 2005 and November 2008 who had resection of a pulmonary nodule pathologically diagnosed as bronchogenic carcinoma or granuloma and preoperative imaging with CT and PET. Each nodule was evaluated on CT for size, doubling time, location, borders, shape, internal characteristics, calcification, clustering, air bronchograms, and cavitation. A diagnostic impression was rendered. Bivariate and logistic regression analyses were performed. Pre-PET data regarding the proportion of resected granulomas and carcinomas between January 1995 and December 1996 were reviewed. RESULTS: Sixty-eight percent (65/96) of nodules were carcinomas and 32% (31/96) were granulomas. The CT impression was benign in 65% (20/31) of granulomas and 5% (3/65) of carcinomas (p < 0.0001; negative predictive value [NPV], 87% [20/23]). Specific CT features significantly associated with granuloma were clustering, cavitation, irregular shape, lack of pleural tags, and solid attenuation. The combination of nonspiculated borders, irregular shape, and solid attenuation had an NPV of 86% (12/14). Granulomas represented 18% (9/50) of resected nodules in 1995 and 1996 (p = 0.066). CONCLUSION: CT findings reduce but cannot eliminate the possibility that a nodule is malignant. Outcomes-based clinical trials are needed to determine whether CT features of benignity can guide less-invasive initial management and reverse a concerning trend in granuloma resection.


Assuntos
Carcinoma Broncogênico/diagnóstico por imagem , Granuloma/diagnóstico por imagem , Neoplasias Pulmonares/diagnóstico por imagem , Tomografia Computadorizada de Emissão , Tomografia Computadorizada por Raios X , Idoso , Carcinoma Broncogênico/cirurgia , Distribuição de Qui-Quadrado , Diagnóstico Diferencial , Feminino , Fluordesoxiglucose F18 , Granuloma/cirurgia , Humanos , Modelos Logísticos , Neoplasias Pulmonares/cirurgia , Masculino , Pessoa de Meia-Idade , Compostos Radiofarmacêuticos , Estudos Retrospectivos
2.
Breast Cancer Res ; 5(2): R52-8, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12631399

RESUMO

BACKGROUND: Molecular genetic markers to identify the 13% lymph node-negative mammary carcinomas that are prone to develop metastases would clearly be of considerable value in indicating those cases in need of early aggressive therapy. METHODS: Representational difference analysis was used in an attempt to identify genetic alterations related to breast cancer metastasis by comparing genomic DNA from microdissected normal cells and from metastatic cells of ductal breast carcinoma patients. RESULTS: Representational difference analysis products yielded 10 unique metastasis-associated DNA sequences (MADS), i.e. products apparently lost in metastatic cell DNA. Of these sequences, MADS-IX was found to be lost in the transition from primary to metastasis in two out of five ductal breast carcinoma cases. This sequence was localized on chromosome 10q21 by radiation hybrid mapping and fluorescence in situ hybridization. The PTEN gene, which is also located on chromosome 10q, was detected to be present by PCR in all five cases. On the contrary, a breast carcinoma cell line, HCC-1937, which has homozygous loss of a region encompassing the PTEN gene, showed the presence of MADS-IX. PCR screening of three additional breast carcinoma cell lines with known losses in specific chromosomal regions also showed the presence of MADS-IX. CONCLUSION: These data suggest that MADS-IX possibly is part of a novel candidate metastasis-associated gene located close to the PTEN gene on chromosome 10q. The first set of PCR screening in five patient samples indicates that it could be used as a molecular marker for ductal mammary metastasis.


Assuntos
Neoplasias da Mama/genética , Carcinoma Ductal de Mama/genética , DNA de Neoplasias/genética , Metástase Neoplásica/genética , Neoplasias da Mama/patologia , Carcinoma Ductal de Mama/patologia , DNA de Neoplasias/química , Feminino , Marcadores Genéticos/genética , Predisposição Genética para Doença/genética , Humanos , Hibridização in Situ Fluorescente , Pessoa de Meia-Idade , Metástase Neoplásica/patologia , PTEN Fosfo-Hidrolase , Monoéster Fosfórico Hidrolases/genética , Mapeamento de Híbridos Radioativos , Análise de Sequência de DNA , Células Tumorais Cultivadas , Proteínas Supressoras de Tumor/genética
3.
Dermatol Surg ; 29(3): 294-6, 2003 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-12614427

RESUMO

BACKGROUND: A case of subungual squamous cell carcinoma, which is a rare malignancy and has an elusive etiology, is reported. OBJECTIVE: To present radiation therapy as a viable treatment option to amputation for surgically unresectable subungual squamous cell cancer. METHODS: A 69-year-old man with a 16-year-old history of subungual squamous cell carcinoma of the left thumb was treated by external beam radiation therapy. In this case, bone invasion precluded the patient from successfully completing Moh's micrographic surgery. RESULTS: The treated thumb at 17 months after radiation therapy remained tumor free. CONCLUSION: Radiation therapy should be considered a treatment option for nail bed squamous cell carcinoma before considering amputation and perhaps as salvage for all unresectable lesions.


Assuntos
Carcinoma de Células Escamosas/radioterapia , Doenças da Unha/radioterapia , Terapia de Salvação , Neoplasias Cutâneas/radioterapia , Idoso , Humanos , Masculino
4.
Cancer Detect Prev ; 27(1): 19-23, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12600413

RESUMO

A dinucleotide (T-G) repeat sequence was isolated by comparing DNA from metastatic lymph node and matched normal breast samples from a ductal mammary carcinoma patient using representational difference analysis (RDA) method. Our present study used this metastasis associated DNA sequence (MADS) as a diagnostic probe to screen five patient samples by slot blot method. A new approach to isolate single cells by microdissection, namely single cell microdissection (SCM) was developed to obtain homogeneous population of tumor cells (approximately 1000) from matched primary tumors and corresponding positive lymph nodes of five patients. We isolated DNA from these homogeneous tumor cells and used for the RDA and DNA slot blot experiments. The screening of patient samples showed loss of this MADS in the transition from primary to metastasis in four out of five cases (80%) suggesting its possible role in breast metastasis.


Assuntos
Biomarcadores Tumorais/genética , Neoplasias da Mama/genética , Carcinoma Ductal de Mama/genética , DNA de Neoplasias/genética , Repetições de Microssatélites/genética , Southern Blotting , Separação Celular/métodos , Marcadores Genéticos , Humanos , Metástase Linfática/genética , Reação em Cadeia da Polimerase
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