scholarly journals Unusual Differential Disease Entity of Right Lower Abdominal Pain, Ileal Diverticulitis Perforation: A Report of Three Cases

2017 ◽  
Vol 102 (11-12) ◽  
pp. 530-535
Author(s):  
Pyong Wha Choi ◽  
Mee Joo

Introduction: Small bowel diverticulum is a rare disease entity, and most cases are asymptomatic. However, diverticulitis can cause acute abdomen conditions like colonic diverticulitis. Depending on the location, various abdominal symptoms may ensue. Clinical manifestations of ileal diverticulitis may be similar to those of appendicitis and or colonic diverticulitis. Thus, making a diagnosis based on a physical examination alone may be challenging. Even though imaging techniques such as computed tomography (CT) may provide clues for a definite diagnosis, the majority of cases are confirmed through operation. Here, we present 3 cases of ileal diverticulitis perforation, which were not diagnosed preoperatively. Case presentation: A 71-year-old man, a 77-year-old woman, and a 78-year-old woman presented with abdominal pain. All 3 patients showed local peritoneal irritation signs in the right lower quadrant. Appendicitis or colonic diverticulitis was suspected, but CT scan results revealed free air and mesenteric fat infiltration around the terminal ileum, suggesting ileal perforation. During the operation in each case, terminal ileal perforation was confirmed, and ileocecal resection was performed. Subsequently, histologic examination revealed ileal diverticulitis perforation. Although the postoperative course was uneventful in the first and second patient, the third patient died of sepsis resulting from anastomosis leakage. Conclusion: These cases put forth unusual causes of right lower quadrant pain, which show physical findings similar to those of diverse inflammatory disease. Awareness of this disease is beneficial for making a differential diagnosis based on CT findings and eliciting prompt surgical management.


2021 ◽  
Vol 9 ◽  
pp. 232470962110224
Author(s):  
Leonidas Walthall ◽  
Marc Heincelman

Pyometra, a purulent infection of the uterus, is a rare cause of a very common complaint—abdominal pain. Risk factors include gynecologic malignancy and postmenopausal status. The classically described presentation includes abdominal pain, fever, and vaginal discharge. In this article, we present an atypical presentation of nonperforated pyometra in an 80-year-old female who was admitted to the internal medicine inpatient service. She initially presented with nonspecific subacute right lower quadrant abdominal pain. Physical examination did not demonstrate vaginal discharge. Laboratory evaluation failed to identify an underlying etiology. Computed tomography scan of the abdomen and pelvis with oral and intravenous contrast demonstrated a 6.5 × 6.1 cm cystic containing structure within the uterine fundus, concerning for a gynecologic malignancy. Pelvis ultrasound confirmed the mass. Endometrial biopsy did not reveal underlying malignancy, but instead showed frank pus, leading to the diagnosis of pyometra. This report illustrates that pyometra should be considered in the differential diagnosis of lower abdominal pain in elderly women.



Author(s):  
Zachary Pacheco ◽  
Peter Abraham ◽  
Brandon Delavar


2020 ◽  
Vol 2020 (2) ◽  
Author(s):  
Floris B Poelmann ◽  
Ewoud H Jutte ◽  
Jean Pierre E N Pierie

Abstract Intestinal obstruction caused by pericecal internal herniation are rare and only described in a few cases. This case describes an 80-year-old man presented with acute abdominal pain, nausea and vomiting, with no prior surgical history. Computed tomography was performed and showed a closed loop short bowel obstruction in the right lower quadrant and ascites. Laparoscopy revealed pericecal internal hernia. This is a viscous protrusion through a defect in the peritoneal cavity. Current operative treatment modalities include minimally invasive surgery. Laparoscopic repair of internal herniation is possible and feasible in experienced hands. It must be included in the differential diagnoses of every patient who presents with abdominal pain. When diagnosed act quick and thorough and expeditiously. Treatment preference should be a laparoscopic procedure.





2021 ◽  
Vol 14 (7) ◽  
pp. e242523
Author(s):  
Samer Al-Dury ◽  
Mohammad Khalil ◽  
Riadh Sadik ◽  
Per Hedenström

We present a case of a 41-year-old woman who visited the emergency department (ED) with acute abdomen. She was diagnosed with perforated appendicitis and abscess formation on CT. She was treated conservatively with antibiotics and discharged. On control CT 3 months later, the appendix had healed, but signs of thickening of the terminal ileum were noticed and colonoscopy was performed, which was uneventful and showed no signs of inflammation. Twelve hours later, she developed pain in the right lower quadrant, followed by fever, and visited the ED. Physical examination and blood work showed signs consistent with acute appendicitis, and appendectomy was performed laparoscopically 6 hours later. The patient recovered remarkably shortly afterwards. Whether colonoscopy resulted in de novo appendicitis or exacerbated an already existing inflammation remains unknown. However, endoscopists should be aware of this rare, yet serious complication and consider it in the workup of post-colonoscopy abdominal pain.



1999 ◽  
Vol 16 (5) ◽  
pp. 441-444 ◽  
Author(s):  
Kazuya Kato ◽  
Minoru Matsuda ◽  
Kazuhiko Onodera ◽  
Hiromi Sakata ◽  
Tatsuo Kobayashi ◽  
...  


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Manabu Kaneko ◽  
Hiroaki Nozawa ◽  
Hirofumi Rokutan ◽  
Koji Murono ◽  
Tetsuo Ushiku ◽  
...  

Abstract Background Ectopic decidua is the presence of decidual tissue outside the uterus. Ectopic decidua of the appendix is a rare entity that can present with abdominal symptoms mimicking appendicitis. We report a case of a 39-year-old female patient at 27 weeks gestational age with a 2-day history of right lower quadrant abdominal pain. Case presentation The patient was referred to our hospital with suspicion of either acute appendicitis or threatened rupture of the uterus, the latter of which was considered unlikely following close examination. Therefore, she underwent emergency appendectomy via laparotomy. Microscopic examination revealed decidual tissue with myxoid degeneration in the subserosal layer of the tip side of the appendix, without endometriosis, which was compatible with ectopic decidua (deciduosis). Conclusions Because it is extremely difficult to distinguish ectopic decidua of the appendix from acute appendicitis, even with various imaging modalities, we should be aware that ectopic decidua of the appendix is a differential diagnosis for acute appendicitis in pregnant women.



Author(s):  
Elina Lietzén ◽  
Paulina Salminen ◽  
Juha M. Grönroos




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