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An Incidental Finding of Concomitant Medullary Thyroid Carcinoma and Papillary Thyroid Carcinoma: A Case Report.
Cureus
November 2024
Department of Internal Medicine, Division of Endocrinology, Ministry of National Guard-Health Affairs, Jeddah, SAU.
Concomitant medullary thyroid carcinoma and papillary thyroid carcinoma in the thyroid gland are rare; however, the incidence is increasing. Here, we present the case of a 77-year-old male who was incidentally found to have thyroid nodules after a road traffic accident. Fine-needle aspiration revealed two inconclusive Bethesda classifications: follicular neoplasm and unsatisfactory.
View Article and Find Full Text PDFMetastatic parathyroid carcinoma diagnosed after five surgical attempts: a case report and review of the literature.
J Cardiothorac Surg
December 2024
Tracheal Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Article Synopsis
- * A 45-year-old woman, initially diagnosed with parathyroid adenoma, experienced a rise in hormone levels 2.5 years post-surgery, leading to further unsuccessful treatments before being referred for additional investigation.
- * Ultimately, the diagnosis of parathyroid carcinoma was made after exploring the mediastinum, revealing metastases rather than the expected thyroid cancer spread, underscoring the need for careful follow-up in hyperparathyroidism cases.
Tracheal diverticula constitute a subtype of paratracheal air cysts that are characterized by a connection with the trachea through a thin neck. Patients with tracheal diverticulum rarely develop symptoms and are usually diagnosed on computed tomography (CT) performed for an unrelated indication. However, identifying the communication with the trachea on imaging may be challenging.
View Article and Find Full Text PDFTracheobronchial Diverticulosis.
J Belg Soc Radiol
November 2024
Department of Radiology, Epidura La Madeleine, Rue Maria Thomée, 1, 7800 Ath, Belgium.
Tracheal diverticulosis is a rare and benign disorder, characterized by single or multiple tracheal wall outpouchings, either congenital or acquired, usually diagnosed incidentally on chest high‑resolution computed tomography, and in general remaining asymptomatic.
View Article and Find Full Text PDFEndotracheal hamartoma causing persistent dyspnoea after coronary artery bypass grafting.
BMJ Case Rep
October 2024
Department of Medicine, University of Florida, Gainesville, Florida, USA.
Article Synopsis
- Pulmonary hamartomas are abnormal growths of mature tissues, typically benign and often found incidentally, but can lead to serious complications like obstruction and infection.
- Tracheal hamartomas, which are very rare, can cause respiratory symptoms such as cough and wheezing, potentially leading to airway obstruction and cardiovascular issues.
- A case report highlights a patient with a tracheal hamartoma misdiagnosed as obstructive pulmonary disease after recent heart surgery, underlining the importance for clinicians to recognize this uncommon condition.
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