2,576 results match your criteria: "Malignant Carcinoid Syndrome"

Gastrointestinal (GI) diseases can present with several extraintestinal manifestations, and cutaneous signs and symptoms are most frequent. Although conventionally GI and skin are considered two entirely separate organ systems, they are closely correlated in origin. An increasing amount of data highlights the complex relationship between GI and dermatological conditions.

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Carcinoid heart findings in vasoactive intestinal peptide-secreting tumour.

BMJ Case Rep

November 2024

Division of Cardiology, Department of Medicine, Harbor-UCLA Medical Center, Torrance, California, USA.

Article Synopsis
  • - Diagnosis of tricuspid valve disease in patients with carcinoid heart syndrome is often done with echocardiography, especially in those already diagnosed with carcinoid syndrome.
  • - VIPoma is a rare type of tumor occurring in 0.05%-2% of cases, causing symptoms like flushing, diarrhea, and electrolyte issues without typically affecting heart valves.
  • - In a notable case, detection of tricuspid regurgitation and stenosis during echocardiography led to a quicker investigation for cancer, ultimately revealing the presence of VIPoma.
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Synchronous bilateral typical pulmonary carcinoid tumours diagnosed by robotic navigation bronchoscopy: A unique case.

Respirol Case Rep

November 2024

Pulmonary and Critical Care Pulmonary and Sleep Physicians of Houston Webster Texas USA.

Article Synopsis
  • * A case study describes a 69-year-old woman with symptoms like flushing, diarrhea, shortness of breath, and cough, leading to the identification of bilateral lung nodules confirmed as carcinoid tumors through biopsy.
  • * The preferred treatment is complete surgical removal of the tumors, but plans are tailored to each patient based on tumor location and lung function, which can complicate surgery.
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Article Synopsis
  • * A study analyzed 165 stage IV SI-NET patients between 2015 and 2021, revealing that 25% developed CHD, particularly moderate-to-severe tricuspid insufficiency, and had a median OS of 4.5 years after CHD diagnosis.
  • * The research highlights the importance of screening and monitoring for CHD in patients with CS, as CHD significantly worsens prognosis, with a hazard ratio for OS
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Horizontal partial laryngectomy for laryngeal neuroendocrine tumor: A case report.

Int J Surg Case Rep

November 2024

Department of Otolaryngology-Head and Neck Surgery, Jichi Medical University, School of Medicine, Shimotsuke 329-0498, Japan. Electronic address:

Article Synopsis
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Article Synopsis
  • The text indicates that a Clinical Vignette is not obligatory for submission or consideration.
  • This suggests that there may be alternative ways to provide relevant information or showcase skills without having to include a vignette.
  • Understanding of this requirement could help streamline the preparation process for students or professionals in the field.
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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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Management of carcinoid heart disease.

Curr Probl Cancer

October 2024

Division of Cardiothoracic Surgery, Department of Surgery, Oregon Health & Science University, Portland, OR, USA. Electronic address:

Carcinoid Heart Disease (CaHD) is defined as the constellation of all cardiac manifestations that occur in patients with carcinoid tumors. Cardiac manifestations are generally due to the paraneoplastic effects of vasoactive substances secreted by carcinoid tumors. These primarily cause cardiac valve dysfunction and resultant heart failure.

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Bronchopulmonary carcinoid tumors are rare, slow-growing malignant neuroendocrine tumors. Early diagnosis is pivotal as surgical resection is the main stay of treatment. A 40-year-old female with typical bronchial carcinoid presented with complaints of breathlessness on mild to moderate exertion, intermittent productive cough, low-grade fever, and loss of appetite since 1 year.

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Background: Carcinoid tumors are rare neuroendocrine malignancies presenting in an increasing number in our center. The incidence of carcinoid tumors is approximatively between 2.5 and 5 cases per 100,000 people of whom about 50% develop carcinoid syndrome.

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Intussusception is a prominent contributor to bowel obstruction, marked by the invagination of a proximal bowel section into a distal segment. Ileocecal intussusception occurs when a portion of the terminal ileum folds into the cecum. In adults, intussusception is infrequent compared to pediatric cases, and represents a minority of bowel obstructions.

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Background: The survival of patients with neuroendocrine tumors has substantially improved with modern treatment options. Although the associated carcinoid syndrome can be diagnosed early and controlled effectively, cardiologists still encounter patients with cardiac manifestations, particularly among individuals with persistently high levels of vasoactive mediators. Treatment options have been limited to surgical valve replacement in fully manifested disease.

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Carcinoid heart disease (CHD) is a frequent and life-threatening complication in patients with carcinoid tumors. Its clinical management is challenging is some cases since serotonin-induced valve fibrosis leads to heart failure. Telotristat is an inhibitor of tryptophan-hydroxylase (TPH), a key enzyme in serotonin production.

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Multiple bronchial carcinoids associated with Cowden syndrome.

Endocrine

June 2024

Department of Medicine and Oncology, ENETS Center of Excellence, Faculty of Medicine, Semmelweis University, Budapest, Hungary.

Article Synopsis
  • Cowden syndrome (CS) is a rare genetic disorder linked to mutations in the PTEN tumor suppressor gene, increasing the risk of various tumors, including thyroid and breast cancers.
  • A case study highlights a 46-year-old man with a history of testicular seminoma and thyroid cancer who was diagnosed with CS through genetic testing that confirmed a PTEN mutation.
  • This patient also exhibited multiple pulmonary carcinoid tumors, marking him as the first reported case of CS linked to these specific tumors, suggesting CS may predispose individuals to multifocal pulmonary lesions.
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Carcinoid Heart Disease.

Radiol Imaging Cancer

January 2024

From the David Geffen School of Medicine at the University of California Los Angeles, 200 Medical Plz, Ste B114, Los Angeles, CA 90095-7370 (S.J.); and Department of Radiology, University of California Los Angeles, Los Angeles, Calif (M.R.B., K.R.).

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Background: Intraoperative carcinoid crisis is typically sudden onset of profound hypotension during operations on patients with neuroendocrine tumors. The crisis was thought to be due to massive release of hormones, and perioperative octreotide was recommended as a prophylaxis against the crisis and as first-line treatment. Recent studies show that octreotide does not prevent the crisis and that no massive release of hormones occurs.

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Article Synopsis
  • * A 53-year-old man with an ileum neuroendocrine tumor and liver metastases developed Hedinger syndrome, experiencing worsening shortness of breath and severe low oxygen levels because of a patent foramen ovale.
  • * Diagnostic imaging, including 99mTc-MAA lung perfusion scintigraphy and 68Ga-FAPI-46 PET/CT, helped identify the right-left blood shunting and the characteristic thickening of heart valves linked to serotonin's effects on fibro
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Carcinoid heart disease is a unique and serious cardiac complication of the neuroendocrine tumour that affects the right side of the heart, especially the tricuspid and pulmonic valves, eventually causing right heart failure. We present a middle-aged man with a history of well-differentiated neuroendocrine tumours of the small intestine with extensive metastases to the liver, mesentery and spine who is receiving monthly octreotide therapy. He presented with generalised fatigue, severe ascites and worsening dyspnoea.

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