RESUMO
RATIONALE AND OBJECTIVES: The authors seek to determine if a new method of combining fluoroscopy and nasogastric biopsy can demonstrate the existence and boundary limits of a known gastric carcinoma or its premalignant conditions. The study is performed in hopes of avoiding unnecessary surgery or limiting resection. METHODS: Two cases are presented to illustrate the technique. The first had a known gastric carcinoma; the other had adenomatous change in the antrum. After topical anesthesia was applied, a nasogastric tube with a coaxial biopsy forceps was inserted. Multiple biopsies were taken in a designed geographic pattern and sent to pathology. The patient with known carcinoma received a total gastrectomy. The specimen was sectioned in the same regions as the biopsies to validate mapping technique. RESULTS: Pathology results for sectioned stomach were nearly identical to the biopsies showing the technique can accurately map the stomach. No adenomatous change in the antrum or other sections of the stomach was observed in the second case. This resulted in the patient being spared gastric resection. CONCLUSIONS: Fluoroscopic-guided gastric mapping can aid in determining the boundaries of a known carcinoma or premalignant conditions. Additional cases and follow-up are necessary.
Assuntos
Adenocarcinoma/diagnóstico por imagem , Fluoroscopia/métodos , Mucosa Gástrica/diagnóstico por imagem , Neoplasias Gástricas/diagnóstico por imagem , Adenocarcinoma/patologia , Idoso , Biópsia , Endoscopia do Sistema Digestório , Gastrectomia , Mucosa Gástrica/patologia , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias Gástricas/patologia , UltrassonografiaRESUMO
We describe a 74-year-old man who presented with multifocal small bowel lesions, a large mesenteric mass, and enlarged mesenteric lymph nodes. In each of the extranodal sites and in two of three regional lymph nodes, there were classic histologic features of marginal zone B-cell lymphoma with adjacent areas of Hodgkin's disease, mixed cellularity subtype. Immunophenotypic analysis in the areas of low-grade B-cell lymphoma of mucosa-associated lymphoid tissue showed immunoreactivity for CD45RB and CD20 in the malignant small cell population. Conversely, the areas of Hodgkin's disease demonstrated positive immunoreactivity for CD15 and CD30 in the Reed-Sternberg cells and variants. Latent membrane protein for Epstein-Barr virus was also positive in the Reed-Sternberg cells and variants.
Assuntos
Doença de Hodgkin/complicações , Neoplasias do Íleo/complicações , Linfoma de Zona Marginal Tipo Células B/complicações , Idoso , Antígenos CD20/análise , Antígenos Virais/análise , Herpesvirus Humano 4/imunologia , Doença de Hodgkin/patologia , Humanos , Neoplasias do Íleo/química , Neoplasias do Íleo/patologia , Técnicas Imunoenzimáticas , Imunofenotipagem , Antígeno Ki-1/análise , Antígenos Comuns de Leucócito/análise , Antígenos CD15/análise , Linfonodos/química , Linfonodos/patologia , Metástase Linfática , Linfoma de Zona Marginal Tipo Células B/química , Linfoma de Zona Marginal Tipo Células B/patologia , Masculino , Proteínas da Matriz Viral/análiseRESUMO
Transient myeloproliferative disorder (TMD) and subsequent acute myeloid leukemia (AML) occur with increased frequency in infants and children with Down syndrome. TMD can also occur in phenotypically normal newborns. We describe the second case of a non-Down syndrome child with TMD who subsequently developed AML. Trisomy 21 karyotypic was restricted to hematopoietic cells in the blood and bone marrow. No other karyotypic abnormalities were found. Leukemic blasts showed megakaryoblastic features with immunophenotyping. This case shows that TMD in a child without Down syndrome may not be entirely benign. Close follow-up is warranted.
Assuntos
Leucemia Megacarioblástica Aguda/genética , Transtornos Mieloproliferativos/complicações , DNA de Neoplasias/genética , Síndrome de Down , Humanos , Lactente , Recém-Nascido , Masculino , Transtornos Mieloproliferativos/congênitoRESUMO
Primary cardiac lymphomas, defined as those involving only the heart and pericardium, are extremely rare tumors. These tumors are commonly fatal and until recently were rarely diagnosed antemortem. We describe the CT and MR findings in a case of primary lymphoma of the heart currently responding to chemotherapy.