Braun David S, Bushe Bryce, Lytvak Irina, Kedia Prashant
Internal Medicine, Methodist Dallas Medical Center, Dallas, TX.
Gastroenterology, Methodist Dallas Medical Center, Dallas, TX.
ACG Case Rep J. 2021 Jan 8;8(1):e00505. doi: 10.14309/crj.0000000000000505. eCollection 2021 Jan.
Pseudomyxoma peritonei (PMP) is a rare clinical condition characterized by a mucin-producing tumor. PMP tumor cells migrate to abdominal and pelvic sites, eventually enveloping intra-abdominal organs and compressing the gastrointestinal tract. Patients with PMP are often asymptomatic in early stages of the disease, but in later stages develop symptoms including abdominal pain, acute abdomen, increased abdominal girth, vomiting, and bowel obstruction. Nonspecific symptoms combined with a relatively modest accuracy of imaging modalities frequently lead to delay in PMP diagnosis and treatment, thereby increasing morbidity. We present a case demonstrating severe erosive esophagitis as a result of PMP-associated gastric antrum compression.
腹膜假黏液瘤(PMP)是一种罕见的临床病症,其特征为产生黏液的肿瘤。PMP肿瘤细胞迁移至腹部和盆腔部位,最终包裹腹内器官并压迫胃肠道。PMP患者在疾病早期通常无症状,但在后期会出现腹痛、急腹症、腹围增加、呕吐和肠梗阻等症状。非特异性症状加上成像方式的准确性相对不高,常常导致PMP诊断和治疗延迟,从而增加发病率。我们报告一例因PMP相关的胃窦压迫导致严重糜烂性食管炎的病例。