Acute Appendicitis with Pyogenic Liver Abscesses


7 min readApr 30, 2024

Acute appendicitis is one of the most common surgical pathologies globally and its treatment has been well practiced for many years. However, clinically it can present in many different ways, from asymptomatic to septic shock and every variation in between. We present the case of a middle-aged man presenting with fever as his only symptom. Upon clinical examination, blood evaluation and imaging, an acute appendicitis with multiple pyogenic liver abscesses were found. The patient underwent surgery with removal of the appendix and drainage of the abscesses. With an antibiotic regiment over several weeks and drainage placement the abscesses could be drained successfully, and the patient remained asymptomatic during the follow-up over 6 weeks.


Acute appendicitis is a very common surgical emergency. The laparoscopic removal is the standard of care all around the world. Despite the discussion of conservative treatment of acute appendicitis with antibiotics, the American College of Surgeons, the European Association of Endoscopic Surgery and the World Society of Emergency Surgery all recommend the treatment by appendectomy [1,2]. In an international collaboration, researchers found that 95.7% of patients with acute appendicitis were treated operatively [1]. The lifetime risk of acute appendicitis is 8.6 percent in males and 6.9 in females [3] and the mortality in developed countries lies between 0.09 and 0.24 percent [4]. Typical complications include the perforation of the appendix (observed in 13–20% of acute appendicitis cases), which can result in peritonitis [5]. More rarely, a perityphlitic abscess can form in the proximity of the appendix. The hematogenic spread of bacteria due to an acute appendicitis is possible and has been described. This can lead to the formation of abscesses in the liver through pyemia of the portal vein [6].

Liver abscesses are relatively rare and present 2.3 cases per 100,000 people [7–9], but they account for 48 percent of visceral abscesses and 13% of intraabdominal abscesses [10]. In half of the cases, an underlying disease of the biliary tract can be identified, and the abscesses are often formed following a pyemia of the portal vein due to bowel leakage and peritonitis [6,7,11]. The most common pathogens are Streptococci, especially the Streptococcus milleri group (S. anginosus, S. constellatus, S. intermedius) [12]. Other pathogens include E. coli, K. pneumoniae and S. aureus [13,14]. The symptoms include fever (90%) and unspecific abdominal complaints (50–75%) (6–8,15). Blood work findings usually include elevated alkaline phosphatase (70–90%), Bilirubin and liver enzymes (50%) [6,7,15].

Case Presentation

A 51-year-old male presented in our emergency department with a 4-day history of fever up to 39.0°C. He did not complain of pain, denied any nausea or diarrhea, and had no urinary symptoms. He had no trouble breathing, no coughing and no throat pain. A Covid-19- PCR-Test was negative. He presented with normal blood pressure, tachycardia with a pulse rate of 126/min, a body temperature of 37.7°C, an oxygen saturation of 97% and a breathing rate of 20 bpm. The patient had no personal history of illnesses, no previous operations and did not take regular medication. A blood sample revealed a leucocyte count of 21.48 G/l with predominantly neutrophil granulocytes (18.85 G/l) and a thrombocytosis of 731 G/l. The Acute-phase proteins were significantly high with a C-reactive protein of 237 mg/l, Procalcitonin of 10.48 ng/ml and Ferritin of 4593 μg/l. He also showed elevated liver enzymes (GOT 97 U/l, GPT 87 U/l) and elevated cholestasis parameters (y-GT 472 U/l, ALP 242 U/l and Bilirubin 47.7 μmol/l) upon which we performed a sonography of the abdomen.

The ultrasound scan showed no evidence of cholecystitis or cholezystolithiasis, but multiple liver lesions, which warranted further investigation by computer tomography. The findings of the CT scan corresponded with the ultrasound images and showed multiple liver lesions and a possible appendicitis. The lesions were located in segment VI (6.4 x 7.2 x 6.1 cm) and subcapsular in the segments VII/VIII (11.0 x 12,1 x 7.3 cm) and were suggestive of liver abscesses. The working diagnosis of acute appendicitis with pyogenic liver abscesses was established. The patient was hospitalized. Blood samples with bacterial cultures, serology for parasites (amoeba, echinococcosis) and viruses (HIV, HAV, HBV, HCV) were obtained and the patient underwent surgery. The diagnostic laparoscopy showed an acute appendicitis without perifocal abscess formation. The appendix was removed at the cecal pole using a linear stapling device (Endo-GIA, 45 mm).

Upon inspection and palpation of the liver perforation of the caudal abscess with purulent discharge occured. A microbiotic sample was obtained and a drainage was placed in the abscess cavity, which quickly collected 300ml of pus. The cranial (subdiaphragmal) liver abscess was left untouched for later interventional drainageplacement. The blood culture showed growth of Streptococcus milleri, which coincided with the findings of the intraoperative sample from the abscess. An intravenous antibiotic regiment with Metronidazol and Ceftriaxon was initiated. 7 days after drain removal the antibiotic treatment with Ceftriaxon was changed to Amoxicillin and Probenecid according to the antibiogramm results.

The histology of the appendix showed pyogenic inflammation with no signs for malignancy, further supporting the working diagnosis of acute appendicitis with hematogenous liver abscesses. The serology (viruses and parasites) results all turned out to be negative. Upon interdisciplinary discussion and according to well established treatment practice [16], the cranial abscess was drained percutaneously (25cm, 10 French), which immediately released 135ml of pus. Further bacteriological samples were obtained, which again confirmed Streptococcus milleri. After a few days the drain was removed after complete drainage.During the hospitalization period, the patient remained afebrile and without any symptoms apart from general fatigue. The patient was discharged from hospital after 15 days with an oral antibiotic regiment containing Metronidazol, Amoxicillin and Probenecid.

Investigation Images (Figures 1 & 2)

Figure 1: 6 weeks course with evident size reduction of the liver abscesses.

Figure 2: Intraoperative situs: Top left and right: Spontaneus perforation of the caudal liver abscess with consecutive drainage insertion. Bottom left: Appendix (stapled and resected, apex on the right, basis on the left). Bottom right: View of the subdiaphragmal abscess with adhesions


Antibiotic Treatment

Ceftriaxon i.v. 2g, 17.05–01.06.2020
(total duration 14d).
Metronidazol i.v. 1500mg, 17.05–20.05.2020
(total duration 3d).
Metronidazol p.o. 500mg, 20.05–08.07.2020
(total duration 49d).
Amoxicillin p.o. 3000mg, 20.05–08.07.2020
(total duration 49d).
Probenecid p.o. 1000mg, 20.05–08.07.2020
(total duration 49d).

Surgical Treatment

1. 17.05.2020: Laparoscopic appendectomy and drainage of liver abscess (total duration of drainage: 8 days).
2. 20.05.2020: Ultrasound-guided drainage of liver abscess (total duration of drainage: 6 days).

Supportive Treatment

1. Respiratory physiotherapy

Outcome and Follow-Up

The patient was seen weekly for follow-up examinations over the course of 6 weeks after discharge. During this period, the patient presented himself once with tachycardia and episodes of sweating in the emergency department. Computer tomography ruled out a pulmonary embolism but showed a thrombus of the medial hepatic vein. Oral anticoagulation with Rivaroxaban 20mg daily was established for a planned total duration of 3 months. The antibiotic treatment was continued until the abscesses could no longer be identified in the CAT scan. The patient remained afebrile and did not show any symptoms, apart from fatigue, during followup. The antibiotic treatment could be discontinued as planned, 7 weeks after initiation.


The treatment of pyogenic liver abscesses consists of abscess drainage and antibiotic therapy [17–20]. The therapeutic approach depends on the number and size of liver abscesses. For single, unilocular abscesses smaller than 5cm in diameter, a percutaneous drainage is indicated. This can either be performed through needle aspiration or catheter placement, both bearing similar success rates [17,21–23]. However, needle aspiration has to be repeated in approximately half of the cases [22–24]. In the case of a single, unilocular abscess bigger than 5cm in diameter, a percutaneous drainage with a catheter placement is recommended. With needle aspiration of these larger abscesses the results show slower abscess drainage, longer time to clinical improvement and more often the need for surgical intervention compared to patients with catheter placement [17]. This management should also be applied to very large abscesses (larger than 10cm in diameter), so called “giant abscesses”. With a size of over 10cm in diameter, the risk of complications, including drainage failure and even sepsis leading to death, become significantly higher [8,24,25]. There have been attempts to manage these abscesses surgically, which have shown a lower rate of treatment failure.

However, no change in mortality, duration of clinical manifestation or rate of complications could be identified in the comparison between percutaneous and surgical drainage [26,27]. The therapeutic approach to multiple abscesses should be made by a multidisciplinary team according to the various capabilities and experiences. The successful percutaneous drainage of multiloculated and multiple abscesses has been described [28], which led to a shift in treatment strategy from surgical to an interventional approach. The empiric antibiotic regiment with ceftriaxone and metronidazole is recommended, such that Streptococci, enteric gram-negative bacilli and anaerobes are covered. Alternative regiments should be applied according to local resistances or probable infection pattern. Antibiotic regiments should generally be continued for a total duration of 4–6 weeks, in patients with incomplete drainage the antibiotic application should be intravenously for the whole duration, whereas patients that showed a positive response to drainage can continue the antibiotic therapy orally after 2–4 weeks of parenteral application [21,29,30].

In the case of our patient, the more caudal abscess perforated spontaneously during a laparoscopy. A drainage was inserted, and microbiological samples were taken, which helped identify the responsible pathogen. According to the stated guidelines, we initiated the antibiotic treatment and inserted a percutaneous drainage of the cranial abscess, which was left untouched during surgery. Our case shows the importance of a multidisciplinary approach and shows the efficacy of surgical as well as interventional percutaneous drainage of liver abscesses.




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