scholarly journals Insulinoma

2020 ◽  
Vol 1 (2) ◽  
pp. 78-85
Author(s):  
Ria Yuniarti ◽  
Suly Auline

A B S T R A C TInsulinoma is a functional neuroendocrine neoplasm consisting of insulin-producingcells, which produce insulin uncontrollably, causing a hypoglycemic syndrome. TheHypoglycemic syndrome is a result of hyperinsulinemia which causes adrenergicsymptoms and neuroglycopenia. The clinical diagnosis is based on the Whipple triad,insulin, and C peptide levels in a 72-hour fasting state. Generally, insulinoma is abenign neoplasm with a proliferation index of Ki-67 <2%. On histological features, thegrowth pattern of the insulinoma is usually trabecular or solid. Some insulinomas showa tubuloacinar growth pattern with psammoma bodies. We reported one case ofinsulinoma in a 65-year-old woman, who had experienced fainting, cold sweats for 3years, especially when the patient ate late or at midnight while sleeping. A CT scanshowed a tumor mass in the pancreas possibly an insulinoma and a pancreatectomywas performed. The results of the histopathological examination are bu following peerunder Insulinoma.

2021 ◽  
pp. jclinpath-2021-207464
Author(s):  
Xiaoli Xu ◽  
Rui Bi ◽  
Ruohong Shui ◽  
Baohua Yu ◽  
Yufan Cheng ◽  
...  

AimsThis study was aimed to investigate the clinicopathological significance of immunohistochemical (IHC) Wilm’s tumour 1 (WT1) expression in invasive breast carcinoma with >90% mucinous components.MethodsOne hundred specimens of invasive breast carcinoma with >90% mucinous component were collected. All H&E-stained slides were reviewed, and the clinicopathological data, including sex, age, tumour size, nuclear grade, histological grade, growth pattern and lymph node (LN) status, were collected. IHC staining of WT1, oestrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) and Ki-67 was performed. Fluorescence in situ hybridisation was used to verify the amplification of the HER2 gene. The relationship between WT1 expression and clinicopathological features was analysed statistically.ResultsWT1 expression was detected in 67% (67/100) of invasive breast carcinoma with >90% mucinous components. WT1 expression was significantly associated with low-to-intermediate nuclear grade/histological grade, ER and PR positivity, HER2 negativity, Ki-67 proliferation index <30% and noLN metastasis (all p<0.001). Micropapillary architecture was observed in 80% of cases. WT1 expression was not significantly correlated with different percentage of micropapillary components (p=0.422). None of the histological grade 3 tumours, tumours with HER2 overexpression/amplification and triple-negative specimens showed WT1 expression.ConclusionsWT1 expression was significantly related with low-intermediate nuclear/histological grade, ER positivity, HER2 negativity, a lower Ki-67 proliferation index and no LN metastasis in invasive breast carcinoma with >90% mucinous component. The micropapillary growth pattern in this type of tumour did not show a specific relationship with WT1 expression.


2021 ◽  
Author(s):  
Qing Xie ◽  
Ming Lu ◽  
Shizhen Zhai ◽  
Rui Guo ◽  
Changzhi Du ◽  
...  

Purpose: To analyze neuroendocrine neoplasm (NEN) bone metastasis (BM) and Gallium-68 (68Ga)-DOTA-TATE performance and to explore their correlation with the immunohistochemical proliferation index (Ki-67). Procedures: A total of 112 patients with BMs were screened from 1082 NEN patients who underwent [68Ga]Ga-DOTA-TATE imaging. All patients had pathological results, and BMs were affirmed by clinical/imaging follow-up of and/or histopathology. The maximum standard uptake value (SUVmax) ratio of BM to normal bone determined for each patient was used in the final analysis. Results: The incidence rate of BMs in NENs was 10.35%. BMs occurred in the spine (75%), pelvis (72.3%), ribs (58%), clavicles and scapulae (41.1%), limbs (37.5%) and skull (28.6%). Most cases were associated with liver metastases (70.5%) and lymph node metastases (65.2%) simultaneously. The SUVmax ratio of G3b (median ratio=3.77, Ki-67>55%) was significantly lower than that of G1 (11.43, Ki-67≤2%) and G2a (11.15, 3%≤Ki-67≤10%) separately P<0.05), while no differences were found for the G2b (8.5, 11%≤Ki-67≤55%) and G3a (6.64, Ki-67>55%) groups. In the total patients there was a significant negative correlation between the SUVmax ratio of BMs to normal bone and Ki-67 (r=-0.267, P<0.01). According to the changes in bone density on computed tomography (CT) scans, the cases were divided into four groups: osteogenesis, osteolysis, no change and a mixed group (median Ki-67: 6.5%, 15%, 12%, and 22.5%). The Ki-67 values were significantly different between the osteogenesis group and the other groups (P<0.05). Conclusion: BM is present in 10.35 % of NEN patients, and most have simultaneous liver and/or lymph node metastases. The occurrence of osteogenesis indicates relativity good differentiation and there is a negative correlation between SUVmax ratio of BMs and NEN proliferation.


2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Giuseppe S. Sica ◽  
Leandro Siragusa ◽  
Bruno Sensi ◽  
Vittoria Bellato ◽  
Pierangela Floris ◽  
...  

Adrenocortical oncocytomas are rare and mostly nonfunctioning neoplasms. We report the case of a 27-year-old woman diagnosed with an ACTH-independent Cushing’s syndrome due to left adrenal oncocytoma. She underwent laparoscopic adrenalectomy. Histopathological examination revealed an oncocytoma of uncertain malignant potential with a low Ki-67 proliferation index, inhibin A positivity, and chromogranin A negativity. Electron micrographs confirmed adrenal oncocytoma cells, characterized by the presence of a large amount of mitochondria. The postoperative course was uneventful, and the patient experienced a progressive regression of Cushing-related symptoms. Periodical follow-ups with MRI and cortisol dosage are required due to the neoplasm’s uncertain malignant potential. Considerations on the diagnosis, pathology findings, clinical remarks, and interventions are made.


2021 ◽  
Vol 8 (4) ◽  
pp. 291-293
Author(s):  
Mecdi Gurhan Balci ◽  
Mahir Tayfur

Objective: The incidence of gastric neuroendocrine neoplasms is less than 1%. They are seen as combined tumors with non-neuroendocrine neoplasms at a rate of approximately 7%. This study aims to share the case of mixed neuroendocrine and non-neuroendocrine cancer with the literature. Case: Endoscopic biopsies were taken from the tumoral mass detected in the gastric cardia region at endoscopy in a 60-year-old male patient that has complaints of weight loss and epigastric pain. Histopathological examination revealed malignant tumor infiltration that consisting of neuroendocrine cells with large nuclei and narrow cytoplasm in some areas and adenoid structures composed of atypical cells with pleomorphic large nuclei in some areas. Strong staining was observed in neuroendocrine areas with neuroendocrine markers such as synaptophysin and Chromogranin. Ki-67 proliferative index and mitotic activity were high in neuroendocrine neoplasm areas. The case was reported as a high-grade neuroendocrine-non neuroendocrine mixed neoplasm. Conclusion: Gastric Mixed Neuroendocrine-Nonneuroendocrine neoplasms are rare cases and correct diagnosis and grading are important in the treatment and patient follow-up protocol.


2018 ◽  
Vol 10 (04) ◽  
pp. 437-442
Author(s):  
Namrata Maity ◽  
Chhanda Das ◽  
Madhumita Mukhopadhyay ◽  
Tamanna Parvin ◽  
Ashis Kumar Saha ◽  
...  

ABSTRACT BACKGROUND: Pediatric renal neoplasms comprise about 7%–8% of all neoplasms in children. Wilms tumour (WT) is the most common among pediatric renal tumours. AIMS AND OBJECTIVES: The study was undertaken to study the epidemiological occurrence of pediatric renal tumours in a tertiary care hospital and to ascertain the validity and reliability of touch smear imprint cytology in intraoperative diagnosis of renal tumours and correlate with subsequent histopathological diagnosis and to assess the expression of proliferation marker Ki-67 in different components and stages of WT. MATERIALS AND METHODS: It was a single-institution-based prospective and observational study, conducted for 2 years (from October 2013 to September 2015) in the department of pathology at our hospital. A total of fifty cases were enrolled in this study, all were below 15 years of age. RESULTS: Imprint cytology showed sensitivity, specificity, and diagnostic accuracy of 83%, 98%, and 95.74%, respectively, in diagnosing benign and malignant renal tumours. There was statistically significant correlation of imprint cytology with confirmatory histopathological examination of excision specimen (P < 0.001). Immunohistochemical analysis of Ki-67 was done in all WT cases. Epithelial component had higher proliferative index than blastemal component with P = 0.0082, which was highly statistically significant. CONCLUSION: Imprint cytology is found to be a less expensive, simple, and rapid method, which can be used as an adjunct to histopathology. Correlation between proliferation index as measured with Ki-67 antibody and tumour stage was found. Ki-67 is thus a relevant marker for assessing the proliferative activity.


2012 ◽  
Vol 3 (2) ◽  
Author(s):  
Hrvoje Čupić ◽  
Tomislav Sajko ◽  
Nikolina Sesar ◽  
Mihovil Ivica ◽  
Leo Pažanin

AbstractGangliogliomas are well differentiated and slowly growing neuroepithelial tumors composed of neoplastic ganglion cells and neoplastic glial cells corresponding mostly to the World Health Organization grade I tumors. However, some of these tumors disclose histologically more malignant glial component and correspond to grade II or grade III tumors. We report a case of left temporal lobe tumor in a 42-year-old woman fulfilling the diagnostic criteria for atypical (grade II) ganglioglioma with high Ki-67 proliferation index and p53 immunoreactive tumor cells. In spite of gross total removal of the tumor, it recurred eight months after surgery. Histopathological examination of the recurrent tumor revealed that it had undergone malignant transformation into a glioblastoma. This case indicates that gangliogliomas with high Ki-67 proliferating index and p53 immunoreactivity should be carefully monitored for recurrence and malignant progression regardless of their morphological grading and seemingly total surgical removal.


2019 ◽  
Vol 42 (2) ◽  
pp. 195-199
Author(s):  
Ivica Gjurovski ◽  
Monika Dovenska ◽  
Slavica Kostadinova Kunovska ◽  
Jordanco Milosevski ◽  
Vesna Levajkovic Trajkov ◽  
...  

Abstract A 15 year old female African lion (Panthera leo) was necropsied after its sudden death. The necropsy showed a mammary gland lesion measuring 10 cm in diameter and numerous white nodules with variable size in the liver, spleen, uterus, lungs and the heart. The histopathological examination showed that the neoplastic formation in the mammary region was a simple tubular carcinoma with metastases on the other organs. Upon immunohistochemical examination, the neoplastic cells expressed cytokeratins while the stroma of the tumour expressed vimentin. The proliferation index Ki-67 was moderate. Based on the macroscopic, histopathological and immunohistochemical findings, the neoplasia was diagnosed as a simple tubular mammary carcinoma.


2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. A998-A998
Author(s):  
Ghadah Al-Naqeeb ◽  
Rabin Neupane ◽  
Neelam Baral ◽  
Faye Gao ◽  
Mark Steves ◽  
...  

Abstract Introduction: Insulinoma is a rare neuroendocrine tumor that may occur sporadically or as part of multiple neuroendocrine neoplasia type 1, with an incidence of 4 per million per year. Given the nonspecific symptoms of hypoglycemia, the diagnosis of insulinoma may be delayed by months, years or even decades. Case Presentation: A 50 year-old Hispanic, Spanish speaking male with a history of hypertension presented with progressive epigastric pain, nausea and bilious vomiting for 2 days. Physical exam was notable for abdominal distention and tenderness. Initial labs showed white blood cells of 19.4 k/uL (4-10.8), glucose of 85 mg/dl (65-140). CT abdomen showed findings consistent with moderate grade small bowel obstruction and normal pancreas. The patient was managed conservatively with nasogastric tube placement and nothing per oral (NPO). Within 8 hours started experience sweating, restlessness, fingerstick glucose was 40 mg/dl. Upon questioning, he reported episodes of lightheadedness, sweating and shakiness 8 years prior to this hospitalization, and he recalled being told that he was hypoglycemic during prior hospitalizations at another institution. He stated he was told to drink juice upon experiencing such symptoms and no work up or diagnostic investigation was recommended. We initiated a hypoglycemia investigation when he was NPO, when serum glucose level of 40 mg/dl. Labs showed insulin level 34 uIU/mL (3-19), free insulin 25 uIU/mL (3-19), C-peptide 3.32 ng/mL (0.81-3.85), beta hydroxybutyrate &lt;0.02 mmol/L (0.02-0.27) and proinsulin of 36.6 pmol/L (3-50) and hemoglobin a1C of 5% (3.8-5.6). Serum screening for hypoglycemic agents was negative. When MRI abdomen was negative for a pancreatic mass. We proceeded with advanced diagnostic imaging with endoscopic ultrasound (EUS) which showed a 26 mm x 19 mm ovoid, hypoechoic mass at the junction of the pancreatic body and tail. Tissue specimen obtained with fine needle aspiration showed grade 1 neuroendocrine neoplasm. The patient underwent distal pancreatectomy and splenectomy with suture repair of the small bowel and left wedge liver biopsy. The pathology showed a well-differentiated neuroendocrine tumor of the pancreas, positive for synaptophysin, chromogranin and CD56 and Ki-67 with proliferation index &lt;2% and no evidence of metastasis to the liver. The patient’s hypoglycemia resolved following surgery and rose to &gt; 200 mg/dL requiring us to begin insulin therapy during the hospital stay before ultimately discharging the patient on metformin for type 2 diabetes. Conclusion: Insulinoma is a rare but treatable neuroendocrine tumor. Early diagnosis is important to avoid adverse clinical events related to hypoglycemia. It is important to maintain a strong clinical suspicion in order to identify and pursue the cause of unexplained hypoglycemia to improve the quality of life of patients with this rare condition.


Author(s):  
V.O. Shaprynsky ◽  
O.A. Kaminsky ◽  
Y.V. Babii

Aim: Investigation of the morphological structure of gastrointestinal leiomyomas which complicated by bleeding, and also reveal the reasons of such complications. Material and methods: There are 36 patients in the study group. All patients were hospitalized in Vinnitsa Regional Clinical Hospital during 2010-2021years with the features of acute gastrointestinal bleeding from the upper gastrointestinal tract. The verification of the tumor was carried out using histopathological and immunohistochemical studies in the postoperative period. According to the results of these studies, all patients were diagnosed with leiomyoma. Results: Among all patients hospitalized with an acute GI bleeding during 2010 - 2021, GI leiomyomas were diagnosed in 0.41%. Men accounted for 56.4%, women - 43.6%. Most of all there were patients aged 50-70 years. The size of the smallest tumor witch removed was 2.5 × 2 cm, the largest - 10 × 8 cm. In our study, leiomyomas that were complicated by bleeding were most often localized in the stomach (88.9%) and duodenum (8.3%), and only in one case (2.8%) in the esophagus. Most of the complicated leiomyomas became leiomyomas of such pathomorphological types as cellular, epitheloid and weird leiomyomas. Their histological structure has its own characteristics. The manifestations of neoangiogenesis and destruction of the blood vessels are clearly visible. There is a thin, it is extensions, all vessels are lacunars and sinusoidal. Also it has sings of angiomatosis. Immunohistochemical analysis of all leiomyomas in the study group showed a positive reaction to smooth muscle actin and desmin, and was negative for CD117 and CD34. In all complicated leiomyomas, the intensity of expression of the immunohistochemical marker of endothelial vessels CD31, which is responsible for the level of vascularization, was high, which confirms the results obtained in histopathological examination. The proliferation index of all complicated leiomyomas was below 5%, which confirms the benign nature of these tumors. But the mean expression level of Ki-67 was statistically higher for complicated leiomyomas. Conclusions: During the histopathological examination it was found that leiomyomas of the proliferative pathomorphological subspecies, which include cellular, epitheloid, and weird leiomyomas, were most often complicated by bleeding. Factors that affect the growth rate of gastrointestinal leiomyomas include the level of proliferative activity of the tumor and the level of its vascularization. Determination of the level of tumor proliferation is performed using the immunohistochemical marker Ki-67, and to determine the level of vascularization is responsible for the immunohistochemical marker CD31. Upper gastrointestinal leiomyomas, which complicated by bleeding were characterized by high levels of Ki-67 and CD31 expression. The obtained research data can be used in the selection of diagnostic and treatment management for patients with leiomyomas of the upper gastrointestinal tract.


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