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Neuroendocrine Tumours: a Literature Review
Neuroendocrine tumours (NETs) are a heterogeneous group of malignant neoplasms with diverse morphology and nomenclature. Well-differentiated NETs were historically termed carcinoid tumours, which entailed abundant confusion and misclassification.
K. V. Menshikov+6 more
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Antagonism of 5-HT7 Receptors as a Promising Target for Gastric Cancer via Apoptotic Pathway. [PDF]
Antagonism of 5‐HT7 receptors as an approach for combating gastric cancer through the apoptotic pathway is targeted. The present study aims to unearth potential avenues for advanced therapeutic strategies in the battle against this devastating disease by exploring the intricate interactions between 5‐HT7 receptors and gastric cancer, as well as ...
Cinar I+6 more
europepmc +2 more sources
Somatostatin analogue is useful in carcinoid crisis for symptom control. Optimal dosing of somatostatin analogues for carcinoid symptoms is not known. This case highlighted management issues using combination short-acting octreotide infusion with long ...
Goh Kian Guan+4 more
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Aspects of classification and diagnostic search for transient and persistent facial erythema
Rosacea is one of the most common conditions on the face. Rosacea affecting the central parts of the face and is characterized by erythema, flushing, telangiectasia; papules and pustules.
T. А. Sysoeva+4 more
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Carcinoid tumors are malignant neuroendocrine tumors arising from Kulchitsky cell. The most common site of primary carcinoid tumors is gastrointestinal tract (64%) followed by respiratory tract (28%).
Rohit Tandon, Ravinder Pal Singh
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Ectopic corticotroph syndrome [PDF]
INTRODUCTION Endogenous Cushing's syndrome is a clinical state resulting from prolonged, inappropriate exposure to excessive endogenous secretion of Cortisol and hence excess circulating free cortisol, characterized by loss of the normal feedback ...
Penezić Zorana+5 more
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Hedinger Syndrome—Lessons Learnt: A Single-Center Experience
Background: Hedinger syndrome (HS) or carcinoid heart disease (CD) is a rare and challenging manifestation of malignant neuroendocrine tumours (NETs) involving the heart.
Mohamed El Gabry+6 more
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Background Multiple endocrine neoplasia type 1 (MEN1) syndrome is usually accompanied by endocrine tumors, but non-endocrine tumors can occur as well. However, the coexistence of MEN1 syndrome and malignant tumor such as low-grade fibromyxoid sarcoma has
Maja Radman, Tanja Milicevic
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BACKGROUND Pulmonary carcinoids are rare, low-grade malignant tumors characterized by neuroendocrine differentiation and relatively indolent clinical behavior.
Carmen Mota Reyes+7 more
semanticscholar +1 more source
Background Carcinoids at atypical sites are rare and mostly asymptomatic. In the majority, they show normal levels of serotonin and its metabolites in plasma and urine, resulting in a relatively late diagnosis and hence guarded prognosis.
Karim G. Moustafa, Gamal M. Saied
doaj +1 more source