Abstract
Carcinoid tumor of the pancreas is extremely rare. This article describes the case of a 22-year-old woman who manifested a typical carcinoid syndrome; a definitive diagnosis of a metastatic carcinoid tumor was made from needle aspiration of a supraclavicular lymph node using morphologic, immunocytochemical, and ultrastructural criteria. The carcinoid tumor was subsequently shown to be of pancreatic origin.
| Original language | English |
|---|---|
| Pages (from-to) | 222-227 |
| Number of pages | 6 |
| Journal | Diagnostic Cytopathology |
| Volume | 3 |
| Issue number | 3 |
| State | Published - Sep 1 1987 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Anatomy
Cite this
Malignant carcinoid of the pancreas : a cytologic, ultrastructural, and immunocytochemical study of a case diagnosed by fine-needle aspiration of a supraclavicular node metastasis. / Khorsand, J.; Katz, R. L.; Savaraj, Niramol.
In: Diagnostic Cytopathology, Vol. 3, No. 3, 01.09.1987, p. 222-227.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Malignant carcinoid of the pancreas
T2 - a cytologic, ultrastructural, and immunocytochemical study of a case diagnosed by fine-needle aspiration of a supraclavicular node metastasis.
AU - Khorsand, J.
AU - Katz, R. L.
AU - Savaraj, Niramol
PY - 1987/9/1
Y1 - 1987/9/1
N2 - Carcinoid tumor of the pancreas is extremely rare. This article describes the case of a 22-year-old woman who manifested a typical carcinoid syndrome; a definitive diagnosis of a metastatic carcinoid tumor was made from needle aspiration of a supraclavicular lymph node using morphologic, immunocytochemical, and ultrastructural criteria. The carcinoid tumor was subsequently shown to be of pancreatic origin.
AB - Carcinoid tumor of the pancreas is extremely rare. This article describes the case of a 22-year-old woman who manifested a typical carcinoid syndrome; a definitive diagnosis of a metastatic carcinoid tumor was made from needle aspiration of a supraclavicular lymph node using morphologic, immunocytochemical, and ultrastructural criteria. The carcinoid tumor was subsequently shown to be of pancreatic origin.
UR - http://www.scopus.com/inward/record.url?scp=0023406968&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0023406968&partnerID=8YFLogxK
M3 - Article
C2 - 3311666
AN - SCOPUS:0023406968
VL - 3
SP - 222
EP - 227
JO - Diagnostic Cytopathology
JF - Diagnostic Cytopathology
SN - 8755-1039
IS - 3
ER -