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http://dx.doi.org/10.1097/00006250-196409000-00028DOI Listing

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Article Synopsis
  • The study focuses on improving diagnostic accuracy for pulmonary sclerosing pneumocytoma (PSP) by analyzing 79 confirmed cases from Zhengzhou University between 2015 and 2023.
  • The analysis revealed a predominance of females, with typical age around 47 years, and noted that 5 cases were initially misdiagnosed as adenocarcinoma and 1 as carcinoid.
  • Key diagnostic features include the observation of dual-cell populations within the tumor and specific histological characteristics such as glandular spaces and surface cell types; recognizing these can help prevent misdiagnosis in needle biopsy specimens.
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Introduction And Importance: Surgeons often need to make intraoperative decisions regarding resection of lung tumors without a preoperative pathological diagnosis. Although intraoperative fine-needle aspiration cytology (FNAC) often provides useful diagnostic information, literatures on its usefulness in pulmonary carcinoids is limited.

Case Presentation: A medical chest radiograph revealed an abnormal shadow in the right upper lung field of a 45-year-old Japanese man.

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Our case presents a unique occurrence marking the first documentation of a connection between a typical carcinoid in the context of diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) and vascular anomalies, including a right-sided aortic arch with Kommerell's diverticulum. Kommerell's diverticulum is a rare congenital anomaly. The lusoria subclavian artery, another developmental anomaly, arises from the right aortic arch instead of the typical left side.

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Background: Celiac disease (CeD) is an autoimmune disorder triggered by the immune response to gluten in genetically predisposed individuals. Recent research has unveiled a heightened risk of developing specific malignant neoplasms (MN) and various malignancies, including gastrointestinal, lymphomas, skin, and others, in individuals with CeD.

Aim: To investigate the prevalence of MN in hospitalized CeD patients in the United States.

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Ovarian carcinoid is a rare well-differentiated neuroendocrine tumor resembling those arising in the gastrointestinal tract. We present a case of ovarian carcinoid with magnetic resonance imaging (MRI) findings. A 50-year-old woman with genital bleeding and severe constipation was referred to our hospital.

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