DiseaseID 2008
嗜银细胞瘤
disease
NCI2016_02D:A carcinoid tumor that shows atypical characteristics and has borderline malignant potential.
Relationship Network
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Disease: 1Symptom: 12Target: 12Links: 24
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 2008
- Core Entity Id
- 2259
- Source Entity Count
- 1
- Preferred Name
- Argentaffinoma
- Name Cn
- 嗜银细胞瘤
- Name Pinyin
- Shi Yin Xi Bao Liu
- Name En
- Argentaffinoma
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Neoplastic Process
- Disgenet Type
- disease
- Mesh Class
- Neoplasms
- Do Class
- Hpo Class
- Neoplasm; Abnormality of the nervous system; Abnormality of the endocrine system
- Mesh Class Name
- Neoplasms
- Hpo Class Name
- Abnormality of the endocrine system; Abnormality of the nervous system; Neoplasm
- Do Class Name
- Disease Definition
- NCI2016_02D:A carcinoid tumor that shows atypical characteristics and has borderline malignant potential.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Argentaffinoma
Role
preferred
Name
Carcinoid Tumor
Role
preferred
Name
Carcinoid, Goblet Cell
Role
preferred
Name
Carcinoid
Role
alias
Name
Carcinoid Tumors
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0100570
Herb
HBDIS000440HBDIS004283HBDIS028558
Me Sh
D002276
Umls
C0007095C0600176
Icd10
D3A.00
Sym Map
SMDE06017SMDE06730
Dis Ge Net
C0007095C0205695C0600176
Umls Sty
T191
Hpo Class
HP:0000707HP:0000818HP:0002664
Me Sh Class
C04
Tcmbank Disease
282134353794
Itcmdb Generated
ITX-DISEASE-A116CCDFF640ITX-DISEASE-BDCB63D7B522ITX-DISEASE-BFA809DDF763
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the endocrine system; Abnormality of the nervous system; Neoplasm
Hpo Disease Class
Neoplasm; Abnormality of the nervous system; Abnormality of the endocrine system
Umls Disease Type
Neoplastic Process
Disease Definition
NCI2016_02D:A carcinoid tumor that shows atypical characteristics and has borderline malignant potential.NCI2016_NCI-GLOSS_1602D:A slow-growing type of tumor usually found in the gastrointestinal system (most often in the appendix), and sometimes in the lungs or other sites. Carcinoid tumors may spread to the liver or other sites in the body, and they may secrete substances such as serotonin or prostaglandins, causing carcinoid syndrome.|NCI2016_CDISC_1602D:A neuroendocrine neoplasm arising from enterochromaffin cells in the gastrointestinal tract and (less common) the bronchi with undetermined malignancy status.|NCI2016_02D:A slow growing neuroendocrine tumor, composed of uniform, round, or polygonal cells having monotonous, centrally located nuclei and small nucleoli, infrequent mitoses, and no necrosis. The tumor may show a variety of patterns, such as solid, trabecular, and acinar. Electron microscopy shows small secretory granules. Immunohistochemical studies reveal NSE, as well as chromogranin immunoreactivity. Malignant histology (cellular pleomorphism, hyperchromatic nuclei, prominent nucleoli, necrosis, and mitoses) can occasionally be seen. Such cases may have an aggressive clinical course. Gastrointestinal tract and lung are common sites of involvement.|MSH2017_2016_08_12:A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182)|MEDLINEPLUS_20151021:<p>Carcinoid tumors are rare, slow-growing cancers. They usually start in the lining of the digestive tract or in the lungs. They grow slowly and don't produce symptoms in the early stages. As a result, the average age of people diagnosed with digestive or lung carcinoids is about 60. </p> <p>In later stages the tumors sometimes produce hormones that can cause carcinoid syndrome. The syndrome causes flushing of the face and upper chest, diarrhea, and trouble breathing. </p> <p>Surgery is the main treatment for carcinoid tumors. If they haven't spread to other parts of the body, surgery can cure the cancer. </p>|HPO2016_07_04:A tumor formed from the endocrine (argentaffin) cells of the mucosal lining of a variety of organs including the stomach and intestine. These cells are from neuroectodermal origin. [HPO:sdoelkens]|CHV2011_02:A usually small, slowly growing tumor usually found in gastrointestinal tract|CHV2011_02:A usually small, slowly growing tumor usually found in gastrointestinal tract|CHV2011_02:A usually small, slowly growing tumor usually found in gastrointestinal tract|CHV2011_02:A usually small, slowly growing tumor usually found in gastrointestinal tract|CHV2011_02:A usually small, slowly growing tumor usually found in gastrointestinal tract|CHV2011_02:A usually small, slowly growing tumor usually found in gastrointestinal tract
Me Sh Disease Class
Neoplasms
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Neoplasms
Umls Semantic Type Name
Neoplastic Process