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Journal of the Belgian Society of Radiology logoLink to Journal of the Belgian Society of Radiology
. 2025 Sep 11;109(1):38. doi: 10.5334/jbsr.4079

Gas-Forming Hepatic Metastases Due to Clostridium septicum Infection: A Rare Case Documented with Sequential CT Imaging

Mattia’s Loverde 1, Dan Truc Nguyen 2, Nasroola Damry 1
PMCID: PMC12428319  PMID: 40949463

Abstract

A rare case of hepatic gas-forming metastases secondary to Clostridium septicum infection is described. A 78-year-old woman was admitted with right lower quadrant abdominal pain and deterioration. Initial imaging revealed a right-sided colonic malignancy with hepatic metastases. Follow-up scans showed gas within metastases and minimal pneumoperitoneum, suggesting bowel perforation. However, blood cultures isolated C. septicum, supporting infected necrotic metastases as the source of free gas.

Teaching point: This case emphasizes the importance of distinguishing infectious intratumoral gas from perforation in oncological patients and provides one of the few reports with sequential imaging of this process.

Keywords: Clostridium septicum, liver neoplasms/secondary, colonic neoplasms/complications, bacteremia

Introduction

Clostridium septicum is a spore-forming Gram-positive anaerobe strongly associated with gastrointestinal and hematologic malignancies [13]. While well described in soft tissues, hepatic gas-forming metastases remain rare and are seldom documented with sequential imaging [4, 5]. Other rare complications include aortitis and emphysematous hepatitis [6, 7]. Presented is a case with infected hepatic metastases, confirmed by blood cultures and repeated CT after suspicion of perforation. The transformation of hepatic metastases in the setting of C. septicum bacteremia is reported, with CT features of pre- and post-infectious stages.

Case Report

A 78-year-old woman without an oncological history was referred to the emergency department on July 9, 2025, due to right lower quadrant abdominal pain and general deterioration. She reported fatigue, anorexia, and fever (39.6°C), without diabetes, corticosteroid use, or prior chemotherapy.

She was malnourished with sarcopenia and acute confusion. On clinical examination, there was tenderness and guarding in the right flank, without signs of acute abdomen. A firm, palpable mass was noted in the right iliac fossa.

Laboratory results showed leukocytosis (23,060/µL), high CRP (186 mg/L), thrombocytosis, anemia, and moderate renal dysfunction. Hepatic enzymes were slightly elevated (ALAT 49 U/L, ALP 226 U/L, GGT 200 U/L, LDH 322 U/L).

CT showed an ascending colonic mass with cecal dilatation (7 cm), multiple hypodense hepatic metastases, and a small paracolic fluid collection, but no free air (Figure 1, first CT).

Figure 1.

Axial CT showing hypodense hepatic lesions without gas; Axial CT showing thickened ascending colon

First contrast-enhanced CT scan (July 9, 2025) showing a thickened ascending colon (white arrow) and hypodense hepatic lesions without gas (red arrows).

Two days later, during the staging work-up, an unenhanced chest CT unexpectedly revealed the presence of air in several of the hepatic metastases as well as minimal pneumoperitoneum. This finding suggested bowel perforation, and an additional contrast-enhanced abdominal CT confirmed intratumoral gas within hepatic metastases and extension into the peritoneal cavity, indicating that the free gas originated from these lesions (Figure 2, follow-up CT).

Figure 2.

Axial CT showing gas in hepatic metastases and minimal pneumoperitoneum; Sagittal CT showing gas in hepatic metastases and minimal pneumoperitoneum

Follow-up CT scan (July 11, 2025) showing gas bubbles in several hepatic metastases (white arrows) and minimal pneumoperitoneum (blue arrows) in axial and sagittal planes.

Blood cultures (on July 10) showed C. septicum. Intravenous cefuroxime and metronidazole were initiated, later switched to oral therapy, with a favorable clinical evolution.

The final diagnosis was C. septicum bacteremia with infection of hepatic metastases and gas production, simulating a perforated colon. The patient refused any further diagnostic or therapeutic intervention. Consequently, no biopsy could be performed.

Discussion

C. septicum infection is a known complication of colorectal cancer, particularly in right-sided tumors [1, 2, 8]. Its gas-generating properties can simulate bowel perforation or abscesses [3, 9]. Hepatic involvement remains rare, particularly in metastatic lesions, and very few reports include sequential imaging documentation [4, 5].

In this case, air in hepatic metastases and pneumoperitoneum initially suggested bowel perforation. However, blood cultures positive for C. septicum indicated bacterial translocation through a compromised mucosa due to subocclusion, with hematogenous seeding.

The right-sided tumor and subocclusion align with patterns described in the literature, associating C. septicum with colonic malignancies [2, 3]. Although histopathological confirmation was not obtained due to the patient’s refusal, the clinical, radiological, and microbiological findings strongly supported the presence of a right-sided colonic malignancy complicated by C. septicum bacteremia. The hematogenous spread is likely to be facilitated by tumor-induced tissue hypoxia and necrosis, which create an ideal anaerobic environment [1, 10].

The gas was confined to known liver metastases, suggesting microbial colonization and anaerobic metabolism in necrotic tumor tissue. This highlights the importance of considering infectious etiologies of intratumoral gas, especially when imaging findings are atypical.

This case documents, through sequential CT, the transformation of hepatic metastases into gas-containing lesions releasing gas into the peritoneum. This observation is rarely documented in the literature [2, 5, 8]. It supports infected metastases as the source of free air rather than perforation and objectivates the importance of early microbiological investigation in oncology patients with unusual metastatic imaging features. Early identification of C. septicum is crucial due to its high mortality. Broad-spectrum antibiotics with anaerobic coverage and surgical intervention when appropriate remain the basis of treatment [8].

Conclusion

This case highlights a rare presentation of C. septicum bacteremia, in which gas formation in hepatic metastases produced pneumoperitoneum simulating bowel perforation. In patients with right-sided colonic tumors and anaerobic bacteremia, infectious transformation of metastases should be considered. Sequential CT imaging provides radiological insight into this transformation and emphasizes timely microbiological investigation of sepsis in an oncological setting.

Competing Interests

The authors have no competing interests to declare.

References

  1. Kornbluth AA, Danzig JB, Bernstein LH. Clostridium septicum infection and associated malignancy: Report of 2 cases and review of the literature. Medicine (Baltimore). 1989;68(1):30–37. 10.1097/00005792-198901000-00002. [DOI] [PubMed] [Google Scholar]
  2. Mirza NN, McCloud JM, Cheetham MJ. Clostridium septicum sepsis and colorectal cancer: A reminder. World J Surg Oncol. 2009;7:73. 10.1186/1477-7819-7-73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Powell MJ, Sasapu KK, Macklin C. Metastatic gas gangrene and colonic perforation: A case report. World J Emerg Surg. 2008;3:15. 10.1186/1749-7922-3-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Vázquez-Melero JA, Carrillo MG, Aretxabala IH, et al. Pneumoperitoneum and gas-forming liver abscesses as initial signs of colorectal liver metastases infected with Clostridium. Case Rep Infect Dis. 2017;2(1):1–5. 10.1089/crsi.2017.0024. [DOI] [Google Scholar]
  5. Mao E, Clements A, Feller E. Clostridium septicum sepsis and colon carcinoma: Report of 4 cases. Case Rep Med. 2011;2011:248453. 10.1155/2011/248453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kirchweger P, Wundsam H, Bosse F, et al. Systematic literature review and meta-analysis of Clostridium septicum aortitis. J Vasc Surg. 2022;76(2):595–604.e1. 10.1016/j.jvs.2022.02.029. [DOI] [PubMed] [Google Scholar]
  7. Al Khatib A, Duboc H, Soliman H. Emphysematous hepatitis due to Clostridium septicum. Clin Gastroenterol Hepatol. 2025;23(4):A32. 10.1016/j.cgh.2024.08.013. [DOI] [PubMed] [Google Scholar]
  8. Larson CM, Bubrick MP, Jacobs DM, et al. Malignancy, mortality and medicosurgical management of Clostridium septicum infection. Surgery. 1995;118:592–597. 10.1016/s0039-6060(05)80023-6. [DOI] [PubMed] [Google Scholar]
  9. Chew S, Lubowski DZ. Clostridium septicum and malignancy. ANZ J Surg. 2001;71:647–649. 10.1046/j.1445-1433.2001.02231.x. [DOI] [PubMed] [Google Scholar]
  10. Kennedy CL, Krejany EO, Young LF, et al. The α-toxin of Clostridium septicum is essential for virulence. Mol Microbiol. 2005;57:1357–1366. 10.1111/j.1365-2958.2005.04774.x. [DOI] [PubMed] [Google Scholar]

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