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Dive into the research topics where Anne Mellon Mogensen is active.

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Featured researches published by Anne Mellon Mogensen.


European Journal of Ultrasound | 2000

Clinical report : contrast enhancement of tumor perfusion as a guidance for biopsy

Nanna Bang; Michael Bachmann Nielsen; Ilse Vejborg; Anne Mellon Mogensen

We describe three cases where biopsies from various tumors were guided by contrast enhancement of tumor perfusion. After i.v. administration of Levovist (Schering AG, Berlin, Germany), the tumors showed both hyper- and hypovascular areas. Biopsies from the latter showed marked necrosis or fibrosis. This may cause biopsies not being conclusive. To ensure fully diagnostic biopsies from irregular tumors we propose the biopsy to be performed from the most vascular part demonstrated by contrast enhancement.


Archive | 1989

Multiple adenomas in terminal ileum 25 years after restorative proctocolectomy for familial adenomatous polyposis

Torben Myrhøj; Steffen Bülow; Anne Mellon Mogensen

A patient with familial adenomatous polyposis was treated with colectomy, mucosal proctectomy, and a straight ileoanal anastomosis in 1962. Thirteen to 21 years later recurrent adenomas developed at the ileoanal anastomosis, and 25 years after the operation multiple adenomas were found in the terminal ileum up to 12 cm from the ileoanal anastomosis. It is concluded that colectomy and mucosal procectomy, with or without an ileoanal reservoir, does not eliminate the future risk of adenoma formation. Thus, this method should be used only in selected polyposis patients


Apmis | 2011

Filiform serrated adenomatous polyposis arising in a diverted rectum of an inflammatory bowel disease patient.

Louise Klarskov; Anne Mellon Mogensen; Niels Jespersen; Peter Ingeholm; Susanne Holck

Klarskov L, Mogensen AM, Jespersen N, Ingeholm P, Holck S. Filiform serrated adenomatous polyposis arising in a diverted rectum of an inflammatory bowel disease patient. APMIS 2011; 119: 393–8.


Pathology Research and Practice | 2009

Biopsies of colorectal clinical polyps – emergence of diagnostic information on deeper levels

Mads Warnecke; Ulla Engel; Inge Bernstein; Anne Mellon Mogensen; Susanne Holck

Although the occasional appearance of a normal histology of biopsies from endoscopic colorectal (CR) polyps is generally held knowledge, its prevalence has rarely been focused on, and the yield of additional sections in such cases has been previously addressed in merely four communications. Hitherto, this issue has not been discussed in the context of the clinical setting. The prime aim of this study was to evaluate the yield of step sectioning CR biopsies, considered non-diagnostic (non-diagnostic biopsies (NDB)) on routine sections. The results are correlated with the indications for endoscopy. Additionally, an appropriate, cost-effective approach for handling NDB was sought. Biopsies from 480 clinical polyps were prospectively evaluated by one of three gastrointestinal pathologists and classified as (a) diagnostic biopsies (DB), comprising neoplastic polyps, hyperplastic polyps (HP), sessile-serrated polyp, other diverse causes of polyp formation and (b) NDB comprising normal histology (group 1), suspicious of either adenoma (group 2) or HP (group 3). Material grouped 1-3 was subsequently step-sectioned (three sections prepared from each of nine additional levels). The biopsy specimens were obtained from 245 endoscopies and stratified in the following categories according to the clinical indications: relevant symptoms (symptomatic, n=127), previously documented sporadic large bowel neoplasia (follow-up, n=99), and documented or presumed hereditary condition that confer an increased risk of CRC (hereditary, n=19, including 15 hereditary non-polyposis colorectal cancer (HNPCC) cases). Sixty-five (13.5%) of the 480 samples were classified as NDB (normal morphology n=49, suspicious of adenoma n=5, suspicious of HP n=11), constituting roughly 10% of all biopsies from the symptomatic and the follow-up categories, 32.1% of samples from the hereditary cases, the difference between the hereditary and the non-hereditary cases being statistically significant (p<0.0001). Upon leveling the 65 NDB, a DB emerged in 24 (36.9%) cases, with no significant difference in the yield in relation to the delineated indication categories. Thereby, diagnostic information was obtained with three additional levels in 15 cases, the remaining 9 cases requiring additional sections, ranging from 4 to 8 levels. The present step sectioning approach implied an extra expense of about 112 US


Acta Cytologica | 2002

Endoscopic ultrasonography-guided fine needle aspiration biopsy for staging malignant melanoma of the esophagus: A case report

Susanne Holck; Mette Siemsen; Dennis Bo Jensen; Anne Mellon Mogensen

for each NDB converted to a DB. The higher prevalence of NDB in relation to genetic disorders probably reflects sampling of particularly diminutive lesions. Given the high yield of step sectioning NDB coupled with an acceptable price, our strategy delineated here is recommended in routine practice with the modification of an initial preparation of sections from merely three levels, and if still non-diagnostic, supplementation with additional five levels.


Virchows Archiv | 1989

Duodenal adenomas in familial adenomatous polyposis: their structure and cellular composition with particular reference to endocrine hyperplasia

Anne Mellon Mogensen; Steffen Bülow; Esther Hage

BACKGROUND Malignant melanoma (MM) rarely involves the esophagus. The outlook is dismal unless lesional tissue is limited to the esophageal wall. Hence, staging prior to extensive surgical intervention is desirable. CASE A 54-year-old male presented with fatigue and melena. A diagnosis of MM primary in the esophagus was rendered on a biopsy of an esophageal polyp. The stage, determined by endoscopic ultrasonography-guided fine needle aspiration biopsy, was advanced. On the basis of this information, it was decided to spare the patient mutilating surgery. CONCLUSION This report confirms the utility of endoscopic ultrasonography-guided fine needle aspiration biopsy in documenting the extent of lesions at sites difficult to access. Thus, management can be improved.


Virchows Archiv | 1989

Electron microscopic studies of endocrine hyperplasia in duodenal adenomas in familial adenomatous polyposis

Anne Mellon Mogensen; Esther Hage; Steffen Bülow

134 duodenal biopsies from 14 patients with familial adenomatous polyposis were evaluated by light microscopy for the presence of adenoma. Staining reactions for endocrine cells were applied. 90 biopsies contained adenoma, almost all of the tubular type (98%) with dysplasia, ranging from mild to moderate. Accompanying hyperplasia of argyrophil and argentaffin endocrine cells was found in 91% and 64% of the adenomas, respectively. Based on histological criteria it is concluded that the risk of carcinoma development in the duodenum could equal that in colon and rectum. The observation of endocrine hyperplasia is new, and further investigations are needed before the significance of this finding can be evaluated.


Journal of Hepato-biliary-pancreatic Surgery | 2004

Idiopathic extensive peliosis hepatis treated with liver transplantation

Masanobu Hyodo; Anne Mellon Mogensen; Peter Nørgaard Larsen; André Wettergren; Allan Rasmussen; Preben Kirkegaard; Yoshikazu Yasuda; Hideo Nagai

Electron microscopical studies on endocrine cell hyperplasia of duodenal adenomas from five patients with familial adenomatous polyposis were performed. All the endocrine cell types normally found in the duodenal mucosa were identified. A constant feature was proliferation of duodenal-enterochromaffin cells but an increase in the number of all other endocrine cell types apart from pyloricgastrin cells and somatostatin cells, was also observed. Certain types of intestinal endocrine cells (the intestinal enterochromaffin cell and the glicentin cell) are rare cells in the normal duodenal mucosa. The finding of these cells may indicate increased biological aggressivity.


Diseases of The Colon & Rectum | 1989

Multiple adenomas in terminal ileum 25 years after restorative proctocolectomy for familial adenomatous polyposis. Report of a case

Torben Myrhøj; Steffen Bülow; Anne Mellon Mogensen


Ugeskrift for Læger | 2009

Lymph node identification in colorectal cancer specimens cases

Schmidt Mb; Engel Uh; Anne Mellon Mogensen; Steffen Bülow; Petersen Ln; Susanne Holck

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Steffen Bülow

University of Copenhagen

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Susanne Holck

Copenhagen University Hospital

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Engel Uh

Copenhagen University Hospital

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Esther Hage

University of Copenhagen

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Ulla Engel

University of Copenhagen

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Ilse Vejborg

University of Copenhagen

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