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DOI: 10.1055/a-2003-9752
Role of transduodenal endoscopic ultrasound-guided fine-needle aspiration/biopsy (EUS-FNA/FNB) for diagnosis of retroperitoneal fibrosis (Ormond’s disease)
Rolle der transduodenalen endosonografischen Feinnadelpunktion zur Diagnosestellung der Retroperitonealfibrose (Morbus Ormond)Abstract
Background Retroperitoneal fibrosis (RPF), often referred to as Ormond’s disease when it is of idiopathic origin, is a rare disease characterized by the presence of inflammatory infiltrates and periaortic masses in the retroperitoneum. For a definite diagnosis, a biopsy and subsequent pathological examination is required. Currently accepted methods for retroperitoneal biopsy include open, laparoscopic, or CT-guided approaches. However, transduodenal endoscopic ultrasound-guided fine-needle aspiration/biopsy (EUS-FNA/FNB) for diagnosis of RPF has attracted only little attention in the literature.
Case Reports We report two male patient cases who presented with leukocytosis, elevated C-reactive protein, and a suspicious retroperitoneal mass of unknown origin on computed tomography. One patient also reported left lower quadrant pain, whereas the other patient suffered from back pain and weight loss. In both patients, idiopathic RPF was successfully diagnosed by using transduodenal EUS-FNA/FNB with 22- and 20-gauge aspiration needles. Histopathology revealed dense lymphocytic infiltrates and fibrosis. The procedures lasted approximately 25 and 20 minutes, respectively, and in both patients no serious adverse events occurred. Treatment included steroid therapy and administration of Azathioprine.
Conclusion We demonstrate that using EUS-FNA/FNB to diagnose RPF is a feasible, fast, and safe method, which should always be considered as a first-line diagnostic modality. Hence, this case report emphasizes that gastrointestinal endoscopists are likely to play an important role in the setting of suspected RPF.
Zusammenfassung
Hintergrund Die Retroperitonealfibrose, bei unbekannter Genese auch Morbus Ormond genannt, ist eine seltene Erkrankung, welche durch das Auftreten entzündlicher paraaortaler Infiltrate und Fibrose im Retroperitonealraum gekennzeichnet ist. Zur definitiven Diagnose bedarf es einer Biopsie der verdächtigen Läsion sowie der anschließenden histopathologischen Untersuchung. Zu den allgemein akzeptierten Methoden für die retroperitoneale Gewebeentnahme zählen die offene, laparoskopische sowie die CT-gesteuerte Biopsie. Die endosonografische Feinnadelpunktion von transduodenal hat in diesem Zusammenhang jedoch bislang überraschend wenig Aufmerksamkeit erregt.
Kasuistiken Wir berichten von 2 männlichen Patienten, die sich mit Leukozytose, erhöhtem C-reaktiven Protein und einer auffälligen retroperitonealen Strukturvermehrung unbekannten Ursprungs in der Computertomografie vorstellten. Ein Patient berichtete von Schmerzen im linken unteren Abdomen, während der andere unter Rückenschmerzen und Gewichtsverlust litt. Bei beiden Patienten konnte ein Morbus Ormond mittels der transduodenalen endosonografischen Feinnadelpunktion unter Verwendung von 22- und 20-Gauge-Aspirationsnadeln diagnostiziert werden. Das Verfahren dauerte jeweils etwa 25 beziehungsweise 20 Minuten und bei beiden Patienten traten keine unerwünschten Komplikationen auf. Zur Behandlung wurden Prednisolon und Azathioprin erfolgreich eingesetzt.
Schlussfolgerung Die Verwendung der transduodenalen endosonografischen Feinnadelpunktion zur Diagnose der Retroperitonealfibrose ist eine praktikable, schnelle und sichere Modalität, die in solchen Fällen immer als Mittel der ersten Wahl in Betracht gezogen werden sollte.
Keywords
Endoscopic Ultrasound-Guided Fine Needle Aspiration - Retroperitoneal Fibrosis - Retroperitoneal Space - Ormond's Disease - EUS - Biopsy - diagnostic imagingSchlüsselwörter
Endosonografische Feinnadelpunktion - Retroperitonealfibrose - Retroperitonealraum - EUS - Morbus Ormond - Biopsie - Bildgebende DiagnostikPublication History
Received: 23 November 2022
Accepted after revision: 21 December 2022
Article published online:
27 March 2023
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