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Clinical Syndromes Related to Gastrointestinal Neuroendocrine Neoplasms
Abstract
Neuroendocrine neoplasms (NENs) comprise a heterogeneous group of tumors derived from multipotent neuroendocrine cells that have the inherent ability to synthesize and secrete a variety of substances (peptides and amines). When these substances are bioactive, NENs can present with a related clinical syndrome (functioning NENs) and/or symptoms of mass effects (functioning and nonfunctioning NENs). NENs differ in their pathogenesis, clinical syndromes produced, aspects of biological behavior and response to certain antitumor treatment. The carcinoid syndrome (CS) is the clinical constellation of secretory diarrhea, flushing, wheezing and dyspnea as a result of serotonin production mainly from small intestinal NENs. Complications of CS are frequent and include extensive mesenteric fibrosis, carcinoid heart disease and the life-threatening carcinoid crisis. A variety of substances (mainly hormones) are produced from NENs originating from the pancreas associated with specific symptoms that can lead to their precise diagnosis. NENs may also secrete substances characteristic of other sites of origin and produce a variety of paraneoplastic syndromes and/or change their secretory status with time. Surgery remains the best option for complete tumor resection and symptom relief. Surgery may also be used when medical treatment fails to obtain control of the symptoms along with cytoreductive techniques. Somatostatin analogs (octreotide and lanreotide) constitute the backbone of medical treatment for the majority of functioning NENs as they can alleviate symptoms, stabilize tumor growth and improve the quality of life. Telotristat etiprate is a novel oral agent that inhibits tryptophan hydroxylase, the key enzyme responsible for serotonin production, and can improve the symptoms of CS. Nonspecific and supportive therapies are also used for refractory cases. In this chapter the clinical features of functioning NENs will be analyzed as well as aspects of their diagnosis based on secretory substances and treatment of the hormonal excess.
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Most symptoms attributable to mast cell activation, such as isolated flushing, pruritus, headache, abdominal pain, or tachycardia, are not specific to mast cells but can be found in other clinical conditions and disorders.
“This is because most symptoms attributable to MCA, such as isolated fl ushing, pruritus, headache, abdominal pain, or tachycardia, are not speci fi c to MCs but can be found in other clinical conditions and disorders as well. 112-118”
From Selecting the Right Criteria and Proper Classification to Diagnose Mast Cell Activation Syndromes: A Critical Review (2021) · cites this paper as [115]
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References 48 · Cited by 50
Metadata
- Authors
- Boutzios, G., & Kaltsas, G.
- Affiliations
- National and Kapodistrian University of Athens (GR)
- Venue
- Frontiers of hormone research
- Publisher
- S. Karger AG
- Published
- 2015
- Volume
- 44
- Pages
- 40-57
- ISSN
- 0301-3073 (ISSN-L)
- 1662-3762
- OpenAlex
- W1187538778
- Cited by
- 50
- References
- 48
- Citations by year
- 2025: 6 · 2024: 4 · 2023: 4 · 2022: 3 · 2021: 8 · 2020: 5 · 2019: 7 · 2018: 3 · 2017: 7 · 2016: 3
- FWCI
- 23.34
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- Frontiers of hormone research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Neuroendocrine Tumor Research Advances
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal Bleeding Diagnosis and Treatment
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
- Keywords
- gastrointestinal neuroendocrine neoplasms, carcinoid syndrome, serotonin, somatostatin analogues, octreotide, lanreotide, tryptophan hydroxylase inhibition, paraneoplastic syndrome, carcinoid heart disease, carcinoid crisis, pancreatic neuroendocrine tumors, hormone excess, tumor resection, mesenteric fibrosis
- MeSH terms
- Gastrointestinal Neoplasms, Humans, Malignant Carcinoid Syndrome, Neuroendocrine Tumors
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