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3.
Adv Clin Path ; 5(1-2): 11-6, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11753829

ABSTRACT

AIMS: We report about two cases of thyroid metastases, with neoplastic thrombosis of the jugular vein, originating from a renal clear cell carcinoma and arising respectively 5 and 18 years after the original nephrectomies. MAIN RESULTS AND CONCLUSIONS: The first patient had also a synchronous transitional cell carcinoma of the bladder and a poorly differentiated prostatic adenocarcinoma, further complicating the location of the primary sources of the metastases. The metastases of the first case were firstly diagnosed by mean of fine needle aspiration biopsy, and subsequently histologically confirmed. Histochemical (diffuse PAS-positive cytoplasms) and immunohistochemical stains (wide spectrum cytokeratins low molecular cytokeratins+, Ck8+, CD10+, Vimentin+, Ck20-, Ck7-, Ck19-, PSA-, thyreoglobulin-, TTF-) performed both on cytologic and histological material helped to define the metastases as oriinating from the renal clear cell carcinoma. For the first patient, the other two possible primary sources were ruled out and a possible primary thyroid tumor with clear cell change was also excluded for both patients.


Subject(s)
Adenocarcinoma, Clear Cell/secondary , Carcinoma, Renal Cell/secondary , Kidney Neoplasms/pathology , Thyroid Neoplasms/secondary , Adenocarcinoma, Clear Cell/chemistry , Aged , Biomarkers, Tumor/analysis , Carcinoma, Renal Cell/chemistry , Carcinoma, Renal Cell/surgery , Carcinoma, Transitional Cell/secondary , Diagnosis, Differential , Humans , Immunohistochemistry , Kidney Neoplasms/chemistry , Kidney Neoplasms/surgery , Male , Neoplasms, Multiple Primary , Prostatic Neoplasms/pathology , Thyroid Neoplasms/chemistry , Urinary Bladder Neoplasms/pathology
8.
Arch Ital Urol Androl ; 73(4): 199-203, 2001 Dec.
Article in Italian | MEDLINE | ID: mdl-11822067

ABSTRACT

The Authors report a rare case of bladder diverticulum with radiological findings compatible with infiltrating bladder cancer and left ureterohydronephrosis. The definitive diagnosis was possible only after surgical intervention with mass removal and histological examination that resulted compatible with bladder diverticulum producing an inflammatory pseudotumor of the wall.


Subject(s)
Diverticulum/diagnosis , Urinary Bladder Diseases/diagnosis , Aged , Humans , Male
10.
Pol J Pathol ; 51(1): 3-8, 2000.
Article in English | MEDLINE | ID: mdl-10833897

ABSTRACT

Fundic gland polyps (FGPs) are tiny multiple sessile polyps of the acid-secreting gastric mucosa. They have been described both in a sporadic form, mainly in middle-aged females, and in a syndromic form, associated with familial adenomatous polyposis (FAP)-Gardner's syndrome and attenuated variants (AFAP). They share the same histology, characterised by superficial and deep cystic dilatations, shortened gastric pits, with an inconspicuous lamina propria. They have been for a long time described as innocuous lesions, but some recent reports have shown that FGPs may harbour dysplastic foci and ultimately (particularly syndromic polyps) gastric cancer. Factors influencing their genesis are unknown. A circulating factor in FAP patients has been postulated and a role of female hormones has been suggested for sporadic FGPs. Whereas patients with sporadic FGPs have normal basal acid output, normal fast serum levels of gastrin and pepsinogen I, the role of gastrin seems crucial for the development of cystic changes in flat body-fundus mucosa, and for the appearance of FGPs in patients with Zollinger-Ellison syndrome. A role of H. pylori induced gastritis has been excluded. Actually, patients with both sporadic and syndromic FGPs appear consistently free from H. pylori colonisation, again for an unknown factor(s). Some recent reports have claimed a role for omeprazole in the genesis of FGPs, a highly controversial issue. Ultimately, the nature of FGPs is still debated: some have interpreted them as hamartomatous lesions, others as a peculiar form of hyperplastic polyp.


Subject(s)
Gastric Mucosa/pathology , Polyps/pathology , Stomach Neoplasms/pathology , Adenomatous Polyposis Coli/pathology , Anti-Ulcer Agents/adverse effects , Female , Gardner Syndrome/etiology , Gardner Syndrome/pathology , Gastric Fundus/pathology , Gastrins/blood , Helicobacter pylori , Humans , Male , Omeprazole/adverse effects , Pepsinogen A/blood , Polyps/etiology , Stomach Neoplasms/etiology , Syndrome , Zollinger-Ellison Syndrome/pathology
17.
Adv Clin Path ; 3(3): 47-53, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10655573

ABSTRACT

AIM: We studied the immunophenotype of 9 cases of secretory meningioma (SM), a rarely reported meningioma variant, characterized by small gland-like lumina filled with a PAS-positive, diastase-resistant substance. METHODS: Three samples of arachnoid tissue and 9 SMs were studied with a panel of monoclonal antibodies (MoAbs) against cytokeratins (Ck) 7,8, 20, vimentin, EMA, CEA and the mucin epitopes sialyl-Tn, Tn, CA19.9, CA125, against the BerEP4 and CD15; 3 colonic adenocarcinomas metastatic to the brain and a case of meningioma with metastasis from a gastric signet-ring cell carcinoma were also studied with the same panel of MoAbs for comparison. RESULTS: The 3 samples of arachnoid cap cells were positive only for EMA and vimentin in the supportive stroma. All 9 SMs resulted Ck7+, Ck8+, Ck20-, EMA+, CEA and mucin epitopes+, confirming at an immunohistochemical level the glandular differentiation. Notable exceptions were the negativity for BerEP4 and CD15 antigens. Conversely, the 3 metastatic colonic adenocarcinomas to the brain were Ck7-, Ck8+, Ck20+, CEA and mucin epitopes+, BerEP4 and CD15+; the gastric signet-ring cell carcinoma metastatic to a meningioma showed the same immunophenotype as the other metastatic adenocarcinomas with the exception of BerEP4 negativity. CONCLUSION: The different pattern of cytokeratin expression (Ck7+/Ck20- for SMs, and Ck7-/ Ck20+ for adenocarcinomas) and the negativity for BerEP4 and CD15 epitopes of SMs, could be relevant for the distinction between SMs and metastatic adenocarcinomas.


Subject(s)
Meningeal Neoplasms/pathology , Meningioma/pathology , Adenocarcinoma/chemistry , Adenocarcinoma/secondary , Antibodies, Monoclonal , Antigens, Neoplasm/analysis , Arachnoid/chemistry , Arachnoid/pathology , Brain Neoplasms/chemistry , Brain Neoplasms/secondary , Colonic Neoplasms/chemistry , Colonic Neoplasms/pathology , Humans , Immunoenzyme Techniques , Immunophenotyping , Meningeal Neoplasms/chemistry , Meningeal Neoplasms/classification , Meningioma/chemistry , Meningioma/classification
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