Case Reports in Surgery
Volume 2015 (2015), Article ID 350573, 3 pages
http://dx.doi.org/10.1155/2015/350573

Case Report

A Case of Pneumococcal Peritonitis after Caesarean Section in a Healthy Woman

Georgios Kourounis,1,2 Yiannis Panayiotou,³ Patrick Paul Tabet,1,2 Brian David Wensley Richards,1,2 Athanasios Petrou,1,3 and Marios Loizou1,3

¹St George’s University of London Programme, University of Nicosia, 93 Agiou Nikolaou Street, Engomi, 2408 Nicosia, Cyprus
²St George’s University of London Medical School, Cranmer Terrace, London SW17 0RE, UK
³Surgery Department, New Nicosia General Hospital, Limassol Old Road No. 215, Strovolos, 2029 Nicosia, Cyprus

Received 5 September 2015; Accepted 5 October 2015

Academic Editor: Tahsin Colak

Copyright © 2015 Georgios Kourounis et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Pneumococcal peritonitis is prevalent in children and adults with comorbidities but extremely rare in healthy adults. Here we describe a case of pneumococcal peritonitis in a previously healthy woman with no known risk factors who presented with constipation, abdominal pain, and distention. Her only past medical history was an uncomplicated C-section two months prior to presentation. A laparotomy revealed a pneumococcal peritonitis without visible source of infection. The patient remained hospitalized until completion of antibiotic regimen with Ceftriaxone and resolution of symptoms. This report adds to the small body of evidence showing possible pneumococcal peritonitis in healthy young adults.

1. Introduction

Streptococcus pneumoniae is a well-known and studied pathogen. It is a leading cause of pneumonia and meningitis worldwide [1, 2] and can rarely be found in the abdominal cavity. Pneumococcal peritonitis is well identified in children [3–7] and in adults with comorbidities [8]. Primary pneumococcal peritonitis in adults is seen in patients with liver cirrhosis [9–12], kidney disease [13], and postgastrointestinal surgery [14], women with genitourinary tract infections [14, 15], and elderly patients with ulcerating gastric diseases [14]. Through our literature review, we were able to find only a few case reports describing primary pneumococcal peritonitis in healthy adults in the absence of any of the previously mentioned conditions [16–18]. Secondary pneumococcal peritonitis is more prevalent and defined as having a clearly identifiable source of infection [16]. It is often linked with prior gastrointestinal infection penetration of the peritoneum [3, 14, 15]. We describe here a healthy woman with pneumococcal peritonitis without a primary source of infection or any comorbidities.

2. Case Report

A 31-year-old woman presented at the emergency department with abdominal pain and constipation. The abdominal pain commenced three days prior to admission, the first two of which were accompanied with diarrhea. The patient did not report any prior gynecological, respiratory, or other complaints. Relevant past medical history included an uncomplicated caesarean section two months prior to presentation. She denied any previous illness including genitourinary infections and gastrointestinal disease.

On examination, the patient was alert and oriented. She had a visibly distended abdomen which was extremely tender to palpation. No ecchymosis or hematomas were seen on inspection. The caesarean section site of incision was healed and clean. On admission, her temperature was 36.6°C. She had a heart rate of 133 beats per minute and a respiratory rate of 30 breaths per minute. Her peripheral white blood cell count was 1.18 × 10³/μL (1.18 × 10⁹/L) with a high neutrophil count of 85.6%. These findings were indicative of systemic inflammatory response syndrome. The C-reactive protein measure was 53.8 mg/dL (538 mg/L). Bowel sounds were markedly reduced and her rectal examination revealed soft stools with no visible signs of blood in them.

After initial investigation with abdominal X-ray showing distended bowel loops with fluid levels (Figure 1), explorative laparotomy was done and revealed pyoperitonitis with patchy inflammation in the pelvis. Ovaries and fallopian tubes appeared edematous and inflamed. Multiple peritoneal lavages were performed and cultures of peritoneal pseudomembranes revealed only Streptococcus pneumoniae, three days later. No other microorganisms were found in the peritoneal cultures. Vaginal swab was negative for Streptococcus pneumoniae. The GI tract revealed no foci of trauma, necrosis, or perforations. Loops of small bowel appeared intact but edematous. The decision was taken to leave the surgical wound open with a medical vacuum system. The patient was then started on Ceftriaxone, 2000 mg twice a day for 10 days, and was transferred to the intensive care unit (ICU). Surgery was resumed 36 hours later and revealed a distinct reduction in pelvic inflammation in the absence of pus. Only few pseudomembranes remained on the walls of the small intestine and the reduction in abdominal contents edema made closure of the surgical wound possible.

Figure 1: Erect abdominal X-ray on admission with distended bowels showing fluid levels.

During her stay in ICU, the patient developed fever and diarrhea. Blood cultures and vaginal swabs were negative, as were the stool samples tested for Clostridium difficile toxins A and B. In the ICU, the patient also developed bilateral pleural effusions which were investigated by microbiology with negative culture results. Her condition improved with continuation of prior antibiotic therapy. She remained in ICU for a total of 6 days before being transferred to the general surgery ward. The patient was eventually discharged 23 days after admission.

3. Discussion

Streptococcus pneumoniae is mainly found in the upper respiratory tract of healthy adults and children [1]. The antibiotic era and the acidic environment of the healthy vagina lead to the rarity of Streptococcus pneumoniae in the normal vaginal flora [19], making the risk of genital infection with this organism extremely rare [19]. During puerperium and pregnancy, the changes to the pH levels in the vagina encourage a change in normal flora allowing Streptococcus pneumoniae to colonize the vagina [19].

Though the route and pathogenesis remain undetermined, it is believed that pneumococci can access the peritoneum via the bloodstream after a pneumococcal respiratory infection, via the lymphatic system and the female genital tract, or transmurally via the gastrointestinal tract [16, 20]. Pneumococcal peritonitis was first described in 1885 by Da Bozzolo [20]. It is classified as either primary or secondary peritonitis and is a surgical emergency. In primary pneumococcal peritonitis there is no other evident site of infection; it is commonly associated with liver and kidney disease [9–13]. Secondary pneumococcal peritonitis is usually caused by a primary gastrointestinal or genitourinary tract infection that penetrated the abdominal cavity [3, 14, 15]. Though rarely seen in adults, primary pneumococcal peritonitis occurs predominantly in women [16]. In our case, the patient had a history of a caesarean section two months prior to presentation; as the postpartum period can last up to 6 months [21], it could have played a role in the pathological process. Another case was reported in a postpartum woman, although in the previous report the women had three previous cesarean sections as sole history that were four, five, and seven years prior to the peritonitis [18].

Bacteremia is a complication frequently seen following a peritoneal infection [16]. This phenomenon was not observed in our patient.

The management of pneumococcal peritonitis includes antimicrobial treatment in combination with surgical intervention. Diagnostic and therapeutic laparotomy should be done to confirm the diagnosis and peritoneal toilet helps to reduce the development of abscess and inflammation [16, 22]. Depending on the cause, both Gram stain and culture may show single or mixed organisms [14, 16]. Analysis of the peritoneal fluid helps in differentiating between primary and secondary peritonitis [16]. Identification of the offending organism and determination of definitive antimicrobial treatment are important due to the increasing prevalence of antibiotic resistant strains of Streptococcus pneumoniae. In our case, similar to previous case reports, Ceftriaxone was found efficacious and it should be used, especially in antibiotic resistant strains [16, 23, 24].

In conclusion, pneumococcal peritonitis in adults, although rare, can be observed in previously healthy young adults without comorbidities or visible primary site of infection [16]. It is more frequently seen in females [16]. The nonspecific clinical symptoms make establishment of the diagnosis difficult. Prognosis is good if management involves the combination of adequate antibiotic cover and surgical treatment [16].

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

Å. Örtqvist, J. Hedlund, and M. Kalin, “Streptococcus pneumoniae: epidemiology, risk factors, and clinical features,” Seminars in Respiratory and Critical Care Medicine, vol. 26, no. 6, pp. 563–574, 2005.

D. van De Beek, J. de Gans, A. R. Tunkel, and E. F. M. Wijdicks, “Community-acquired bacterial meningitis in adults,” The New England Journal of Medicine, vol. 354, no. 1, pp. 44–53, 2006.

W. F. Annand and W. H. Bowen, “Pneumococcal peritonitis,” The Lancet, vol. 1, pp. 1591–1597, 1906.

L. E. Barrington-Ward, “Pneumococcal and Streptococcal peritonitis,” BMJ, vol. 2, no. 3745, pp. 704–706, 1932.

W. H. Cole, “Pneumococcal peritonitis,” Surgery, vol. 1, no. 3, pp. 386–394, 1937.

R. Fowler, “Primary peritonitis: changing aspects 1956–1970,” Australian Paediatric Journal, vol. 7, no. 2, pp. 73–83, 1971.

J. E. McCartney and J. Fraser, “Pneumococcal peritonitis,” British Journal of Surgery, vol. 9, no. 36, pp. 479–489, 1922.

T. Skau and Y. Tegner, “Spontaneous peritonitis and rheumatoid arthritis—a case report,” Acta Chirurgica Scandinavica, vol. 152, no. 4, pp. 317–318, 1986.

C. M. Wilcox and W. E. Dismukes, “Spontaneous bacterial peritonitis. A review of pathogenesis, diagnosis, and treatment,” Medicine, vol. 66, no. 6, pp. 447–456, 1987.

J. P. Correia and H. O. Conn, “Spontaneous bacterial peritonitis in cirrhosis: endemic or epidemic?” Medical Clinics of North America, vol. 59, no. 4, pp. 963–981, 1975.

M. Epstein, F. M. Calia, and G. J. Gabuzda, “Pneumococcal peritonitis in patients with postnecrotic cirrhosis,” The New England Journal of Medicine, vol. 278, no. 2, pp. 69–73, 1968.

D. N. Kerr, D. T. Pearson, and A. E. Read, “Infection of ascitic fluid in patients with hepatic cirrhosi,” Gut, vol. 4, pp. 394–398, 1963.

M. Pahmer, “Pneumococcus peritonitis in nephrotic and non-nephrotic children. A comparative clinical and pathologic study with a brief review of the literature,” The Journal of Pediatrics, vol. 17, no. 1, pp. 90–106, 1940.

O. Capdevila, R. Pallares, I. Grau et al., “Pneumococcal peritonitis in adult patients: report of 64 cases with special reference to emergence of antibiotic resistance,” Archives of Internal Medicine, vol. 161, no. 14, pp. 1742–1748, 2001.

H. Westh, L. Skibsted, and B. Korner, “Streptococcus pneumoniae infections of the female genital tract and in the newborn child,” Reviews of Infectious Diseases, vol. 12, no. 3, pp. 416–422, 1990.

C. Hemsley and S. J. Eykyn, “Pneumococcal peritonitis in previously healthy adults: case report and review,” Clinical Infectious Diseases, vol. 27, no. 2, pp. 376–379, 1998.

M. G. Davies, D. P. Halpin, P. O'Byrne, and R. B. Stephens, “Primary pneumococcal peritonitis—a brief report,” Irish Journal of Medical Science, vol. 158, no. 12, pp. 307–309, 1989.

G. W. Christopher, J. A. Hucker, D. W. White, and B. L. Carter, “Pneumococcal infections of the female genital tract,” Reviews of Infectious Diseases, vol. 12, no. 6, pp. 1203–1204, 1990.

E. Madhusudhan, T. S. Kuruvilla, and S. Chandrakar, “Streptococcus pneumoniae: an unusual pathogen seen in high vaginal swab,” International Journal of Biomedical Research, vol. 6, no. 4, pp. 285–287, 2015.

R. Ron-El, I. Bukovsky, J. Kharasch, Y. Letko, and E. Caspi, “Pneumococcal peritonitis with the presence of an intrauterine device,” International Journal of Gynecology and Obstetrics, vol. 23, no. 4, pp. 339–341, 1985.

M. Romano, A. Cacciatore, R. Giordano, and B. La Rosa, “Postpartum period: three distinct but continuous phases,” Journal of Prenatal Medicine, vol. 4, no. 2, pp. 22–25, 2010.

J. M. Muray, D. Galli-Douani, N. Ciraru-Vigneron, and J. Barrier, “Pneumococcal peritonitis. An unusual diagnosis in gynecology,” Journal de Gynécologie Obstétrique et Biologie de la Reproduction, vol. 11, no. 7, pp. 829–832, 1982.

P. D. Lister, “Multiply-resistant pneumococcus: therapeutic problems in the management of serious infections,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 14, supplement 1, pp. 18–25, 1995.

I. R. Friedland and G. H. McCracken Jr., “Management of infections caused by antibiotic-resistant Streptococcus pneumoniae,” The New England Journal of Medicine, vol. 331, no. 6, pp. 377–382, 1994.