Literature DB >> 15619202

Siegfried Oberndorfer: origins and perspectives of carcinoid tumors.

Irvin M Modlin1, Michael D Shapiro, Mark Kidd.   

Abstract

Carcinoid tumors are rare, indolent neoplasms that, although clinically well defined, are regarded as exotic and are consequently often unrecognized. Although little is known of the lives of the men who defined the tumor, described its distinct histology and cell type, and delineated the clinical hallmarks of the disease even less is known of the pathobiology of the lesion. In the nineteenth century, T. Langhans (1839-1915), O. Lubarsch (1860-1933), and W. B. Ransom (1860-1909) described unusual tumors in the small bowel but each failed to adequately investigate these novel entities. This responsibility fell to Siegfried Oberndorfer (1876-1944), who became the first to adequately characterize the nature of the tumors and refer to them as "benign carcinomas." During his tenure at the Pathological Institute of the University of Munich, Oberndorfer noted in 1907 that the lesions were distinct clinical entities and named them "karzinoide" ("carcinoma-like"), emphasizing in particular their benign features. In 1929 he amended his classification to include the possibility that these small bowel tumors could be malignant and also metastasize. Although the enterochromaffin cell, the carcinoid cell of origin, had been identified as early as 1897 by N. Kulchitsky (1856-1925), it was not until 1953 that F. Lembeck (1922-) established that such cells synthesized and secreted serotonin--a potent bioactive amine. Thereafter the protean clinical effects of serotonin, including "flushing," were recognized as was the associated relationship of carcinoid heart disease (Biörck in 1952) and fibrosis (Moertel in 1961). As the centennial of the observations of Oberndorfer approaches, it should be noted that the legacy of one of Germany's most distinguished pathologists, teachers, and scientists (whose career fell victim to the machinations of the Third Reich) has been largely unrecognized. Similarly, the biology and mechanistic analysis of these lesions remain to a large extent unexplored. The present article describes the contributions of the clinical and scientific pioneers in the elucidation of carcinoid disease and traces the evolution of the discovery and understanding of carcinoid tumor biology. It also serves to memorialize the extraordinary accomplishments of Oberndorfer, whose vision exceeded his times.

Entities:  

Mesh:

Year:  2004        PMID: 15619202     DOI: 10.1016/j.humpath.2004.09.018

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  28 in total

Review 1.  Paracrinicity: the story of 30 years of cellular pituitary crosstalk.

Authors:  C Denef
Journal:  J Neuroendocrinol       Date:  2008-01       Impact factor: 3.627

Review 2.  Siegfried Oberndorfer: a tribute to his work and life between Munich, Kiel, Geneva, and Istanbul.

Authors:  Günter Klöppel; Katherine Dege; Wolfgang Remmele; Yersu Kapran; Sitki Tuzlali; Irvin M Modlin
Journal:  Virchows Arch       Date:  2007-08-08       Impact factor: 4.064

Review 3.  Progress and challenges in neuroendocrine and neural crest tumours: molecular imaging and therapy.

Authors:  Giovanni Lucignani; Emilio Bombardieri
Journal:  Eur J Nucl Med Mol Imaging       Date:  2009-12       Impact factor: 9.236

4.  Role of German-speaking scholars in the development of pathology in Turkey.

Authors:  Nadir Paksoy
Journal:  Wien Med Wochenschr       Date:  2019-02-18

Review 5.  Principles of diagnosis and management of neuroendocrine tumours.

Authors:  Michael J Raphael; David L Chan; Calvin Law; Simron Singh
Journal:  CMAJ       Date:  2017-03-13       Impact factor: 8.262

6.  Healthcare and economic impact of diarrhea in patients with carcinoid syndrome.

Authors:  Michael S Broder; Eunice Chang; Dorothy Romanus; Dasha Cherepanov; Maureen P Neary
Journal:  World J Gastroenterol       Date:  2016-02-14       Impact factor: 5.742

7.  Appendiceal neuroendocrine tumors: Recent insights and clinical implications.

Authors:  John Griniatsos; Othon Michail
Journal:  World J Gastrointest Oncol       Date:  2010-04-15

Review 8.  Fibrosis and carcinoid syndrome: from causation to future therapy.

Authors:  Maralyn Druce; Andrea Rockall; Ashley B Grossman
Journal:  Nat Rev Endocrinol       Date:  2009-05       Impact factor: 43.330

Review 9.  Appendiceal carcinoid tumor in children: implications for less radical surgery?

Authors:  A D Malkan; F N Wahid; I Fernandez-Pineda; J A Sandoval
Journal:  Clin Transl Oncol       Date:  2014-06-26       Impact factor: 3.405

10.  Requiem for the term 'carcinoid tumour' in the gastrointestinal tract?

Authors:  Runjan Chetty
Journal:  Can J Gastroenterol       Date:  2008-04       Impact factor: 3.522

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.