National Cancer Institute®
Last Modified: August 1, 2002
1
UI - 12097278
AU - Goebel SU; Iwamoto M; Raffeld M; Gibril F; Hou W; Serrano J; Jensen RT
TI -
Her-2/neu expression and gene amplification in gastrinomas: correlations
with tumor biology, growth, and aggressiveness.
SO - Cancer Res 2002 Jul 1;62(13):3702-10
AD - Digestive Diseases Branch, National Institute of Diabetes and Digestive
and Kidney Diseases, NIH, Bethesda, Maryland 20892-1804, USA.
A proportion of gastrointestinal neuroendocrine tumors are aggressive;
however, little is known of molecular determinants of their growth, and
molecular studies have identified no useful prognostic factors.
Overexpression of HER-2/neu is common in some nonendocrine tumors,
frequently correlates with increased tumor aggressiveness, and can be
used as a basis of treatment with trastuzumab. Little is known of its
expression in malignant pancreatic endocrine tumors. In the present
study HER-2/neu gene amplification and expression was determined in 43
gastrinomas from different patients. Results were correlated with
clinical, laboratory, and tumor characteristics including tumor growth.
HER-2/neu gene amplification was assessed by differential PCR, mRNA
levels assessed by quantitative PCR, and protein by
immunohistochemistry. Fourteen percent of patients had HER-2/neu gene
amplification in tumors compared with levels in their WBCs. HER-2/neu
mRNA varied over a 700-fold range. However, only 3% exceeded levels seen
in normal pancreas, and immunohistochemistry did not show protein
overexpression in any tumor (n = 10). HER-2/neu mRNA levels were
significantly higher (P = 0.032) in tumors associated with liver
metastases but not with tumor location or size. These results show that
HER-2/neu amplification/overexpression does not seem to play a role in
the molecular pathogenesis of most gastrinomas, as suggested in a
previous study involving small numbers of cases. However, mild gene
amplification occurs in a subset, and overexpression is associated with
aggressiveness. Therefore, HER-2/neu levels could have prognostic
significance as well as identify a patient subset with gastrinomas who
might benefit from trastuzumab treatment.
2
UI - 11942775
AU - Eledrisi MS; Stuart CA; Alshanti M
TI -
Insulinoma in a patient with tuberous sclerosis: is there an
association?
SO - Endocr Pract 2002 Mar-Apr;8(2):109-12
AD - Department of Internal Medicine, Division of Endocrinology and
Metabolism, University of Texas Medical Branch, Galveston, Texas 77555,
USA.
OBJECTIVE: To describe a patient with tuberous sclerosis who, on initial
assessment, had neurologic symptoms, which were ultimately found to be
caused by an insulinoma. METHODS: We present a case report with
clinical, laboratory, and radiologic data. The literature is reviewed
relative to tuberous sclerosis and islet cell tumors, and a possible
association is discussed. RESULTS: A 43-year-old man with a history of
tuberous sclerosis required medical attention because of mental
confusion and slurred speech and was found to have hypoglycemia.
Neuroradiologic imaging showed no new lesions to account for his
symptoms. His physical examination was striking for a large abdominal
mass, which showed increased uptake on octreotide scanning. After
surgical resection, the mass measured 21 cm and was found to be an
insulinoma. Blood glucose values were normal postoperatively and on
follow-up, and the patient had no recurrence of the symptoms.
CONCLUSION: From this report, we emphasize two findings. First, we draw
clinicians' attention to the possibility of an association between islet
cell tumors and tuberous sclerosis and suggest consideration of this
diagnosis in patients with tuberous sclerosis who have new or worsening
neurologic symptoms. Second, the insulinoma we describe is, to our
knowledge, the largest to be reported thus far in the literature.
3
UI - 12004358
AU - Jhala D; Eloubeidi M; Chhieng DC; Frost A; Eltoum IA; Roberson J; Jhala
TI -
N
Fine needle aspiration biopsy of the islet cell tumor of pancreas: a
comparison between computerized axial tomography and endoscopic
ultrasound-guided fine needle aspiration biopsy.
SO - Ann Diagn Pathol 2002 Apr;6(2):106-12
AD - Division of Anatomic Pathology, Department of Pathology, University of
Alabama at Birmingham, 35249, USA.
The objective of the present study is to compare the cytologic features
of islet cell tumor (ICT) of pancreas obtained by endoscopic ultrasound
guided fine needle aspiration (EUS-FNA) and computed tomography guided
FNA (CT-FNA). We also describe the cytologic features associated with
malignant ICT. Eleven cytology samples from 121 CT- FNA and 30 EUS- FNA
of the pancreas were obtained from nine patients with ICT. Diff-Quik,
Papanicolaou, and immunohistochemical stains to determine neuroendocrine
differentiation and the hormonal status were evaluated. Cytologic
features and specimen adequacy were compared between the two techniques.
Cytologic features noted in both benign and malignant ICT were also
compared. Nine patients (5 men, 4 women) ranging in age from 29 to 84
years (mean age, 53.8 years). Diagnoses consisted of benign (4) and
malignant (5) ICT. EUS-FNA was superior to CT-FNA in obtaining adequate
cells (2/2 v 7/9) for the diagnosis and increased cellularity to perform
additional immunohistochemical stains (2/2 v 4/7). Single, plasmacytoid
cells with finely granular chromatin distribution characterized ICT on
cytology. Mitoses (3/5) and necrosis (1/5) were noted in malignant ICT
but not in benign ICT. EUS-FNA is superior to CT- FNA for obtaining
cells for the diagnosis of ICT. Detection of mitoses and or necrosis
from patients with ICT should initiate a search for metastasis.
Copyright 2002, Elsevier Science (USA). All rights reserved.
4
UI - 12170715
AU - Naribayashi Y; Tai S; Nakata Y; Yokogawa S
TI -
[A case of small pancreatic glucagonoma detected by health care]
SO - Nippon Shokakibyo Gakkai Zasshi 2002 Jul;99(7):838-42
AD - Department of Internal Medicine, Chibune General Hospital.
5
UI - 12070411
AU - Mirallie E; Pattou F; Malvaux P; Filoche B; Godchaux JM; Maunoury V;
TI -
Palazzo L; Lefebvre J; Huglo D; Paris JC; Carnaille B; Proye C
[Value of endoscopic ultrasonography and somatostatin receptor
scintigraphy in the preoperative localization of insulinomas and
gastrinomas. Experience of 54 cases]
SO - Gastroenterol Clin Biol 2002 Apr;26(4):360-6
AD - Service de Chirurgie Generale et Endocrinienne, Clinique Chirurgicale
Adultes Est, Hopital Claude Huriez, CHU Lille, France.
AIM: The classic morphological techniques for the localization of
insulinomas and gastrinomas are of limited value. Endoscopic
ultrasonography and somatostatin receptor scintigraphy have shown high
sensitivity for the detection of gastroenteropancreatic endocrine
tumors. The aim of the study was to evaluate the sensitivity of
endoscopic ultrasonography and that of somatostatin receptor
scintigraphy in the localization of insulinomas and gastrinomas.PATIENTS
AND METHODS: This retrospective study concerned 54 patients with
examinations. Forty-two patients had scintigraphy (17 with insulinoma,
25 with gastrinoma), 47 had endoscopic ultrasonography (28 with
insulinoma, 17 with gastrinoma). One of the ten patients with MEN 1 had
both tumors. All diagnosis were confirmed by histologic
examination.RESULTS: The sensitivity of scintigraphy for the
localization of insulinomas was 47%. There was one false positive.
Sensitivity of endoscopic ultrasonography for insulinomas was 85%. The
sensitivity of scintigraphy in the detection of gastrinomas was 65% for
the tumors in the duodenopancreatic area, 20% for the tumors in the
pancreatic tail and 71% for metastasis. The sensitivity of endoscopic
ultrasonography was 46% for duodenal tumors, 75% for pancreatic tumors
and 57% for lymph node metastasis. The combination of both localization
studies increased sensitivity to 94%.CONCLUSION: Endoscopic
ultrasonography and somatostatin receptor scintigraphy are the gold
standard for localization of gastrinomas. Association of both
examinations increases the sensitivity. Scintigraphy for the detection
of insulinomas should be performed when endoscopic ultrasonography is
negative.
6
UI - 12142749
AU - Kouraklis G; Stamoulis J; Tassiopoulos S; Glinavou A; Hatzinikolaou P
TI -
Islet cell carcinoma of the pancreas presenting as chylous ascites.
SO - Pancreas 2002 Aug;25(2):213-5
AD - Second Department of Propedeutic Surgery, Medical School, University of
Athens, Athens, Greece.
7
UI - 12001691
AU - Kuzin NM; Egorov AV; Gurevich LE
TI -
[Life-term diagnosis and treatment of malignant vipoma of the pancreas]
SO - Khirurgiia (Mosk) 2002;(4):77-9
8
UI - 11972219
AU - Mahon D; Allen E; Rhodes M
TI -
Laparoscopic distal pancreatectomy. Three cases of insulinoma.
SO - Surg Endosc 2002 Apr;16(4):700-2
AD - Department of Surgery, Norfolk & Norwich University Hospital NHS Trust,
Norwich NR1 3SR, England, UK.
BACKGROUND: Surgery for benign pancreatic disease has traditionally
required a major laparotomy however the minimal-access approach is now
being applied to a wide variety of procedures, and surgery of the
pancreas need not be excluded. METHODS: Laparoscopic distal
pancreatectomy was performed on three patients presenting with
insulinomas found on preoperative investigation to lie within the tail
of the pancreas. RESULTS: All three patients had an excellent clinical
outcome and returned to a state of normoglycemia. All of them made a
rapid recovery with no major complications. CONCLUSION: Laparoscopic
distal pancreatectomy is a viable technique for removing insulinoma of
the tail of the pancreas.
9
UI - 12173721
AU - Dionisi S; Minisola S; Pepe J; De Geronimo S; Paglia F; Memeo L;
TI -
Fitzpatrick LA
Concurrent parathyroid adenomas and carcinoma in the setting of multiple
endocrine neoplasia type 1: presentation as hypercalcemic crisis.
SO - Mayo Clin Proc 2002 Aug;77(8):866-9
AD - Department of Clinical Sciences, University of Rome La Sapienza, Italy.
We describe a patient with multiple endocrine neoplasia type 1
characterized by the simultaneous occurrence of parathyroid cancer,
parathyroid adenomas, and pancreatic gastrinoma, who presented with an
episode of acute hypercalcemia. The rapid parathyroid hormone assay
provided a basis for the diagnosis of parathyroid hyperfunction.
Mediastinal metastasis of the parathyroid carcinoma was found at
autopsy. However, the staining of pancreatic and gastric tissue for
parathyroid hormone-related protein does not make it possible to exclude
completely the contribution of this peptide in mediating the
hypercalcemia. To our knowledge, this is the first reported case of
parathyroid carcinoma as part of the multiple endocrine neoplasia type 1
syndrome.
The above citations and abstracts reflect those newly added to CANCERLIT for the month and topic listed in the title. The citations have been retrieved from CANCERLIT using a predefined search strategy of indexed subject terms. Although the search strategy has been refined as best as possible, citations may appear that are not directly related to the topic, and occasionally relevant references may be omitted.