Skip to main content

Fatal non-thrombotic pulmonary embolization in a patient with undiagnosed factitious disorder



Factitious fever is extremely challenging to diagnose in patients with complicated chronic medical problems, and represents as much as 10% of fevers of unknown origin. Factitious fever caused by self-injecting oral medications through indwelling central catheters is a diagnostic challenge.

Case presentation

We present a 32-year-old Caucasian female with history of short gut syndrome, malnutrition requiring total parental nutrition, and pancreatic auto-islet transplant with fever of unknown origin. Multiple episodes of bacteremia occurred with atypical pathogens, including α-hemolytic Streptococcus, Achromobacter xylosoxidans, and Mycobacterium mucogenicum. Chest computed tomography was notable for extensive tree-in-bud infiltrates. Sudden cardiac arrest with right-sided heart failure following acute hypoxemia led to her death. Diffuse microcrystalline cellulose emboli with foreign body granulomatosis was found on autopsy. Circumstantial evidence indicated that this patient suffered from factitious disorder, and was self-injecting oral medications through her central catheter.


A high index of suspicion, early recognition, and multifaceted team support is essential to detect and manage patients with factitious disorders before fatal events occur.


Fever of unknown origin (FUO) is defined as a fever for 3 or more weeks with a diagnosis that remains uncertain after 1 week of investigation. Due to improved diagnostic testing over several decades infectious and neoplastic causes of FUO have declined while unidentified causes have increased [1]. Factitious fever represents 1–10% of FUO cases [2, 3]. The most comprehensive review of factitious fevers, published in 1979, included 32 cases [3]. Polymicrobial bacteremia from self-injection occurred in five subjects from this study, and has also been reported in other sporadic case reports [4, 5]. All of these studies were published prior to the widespread use of long-term central line catheters, which are routinely used in clinical practice today. Central line-related bloodstream infections are responsible for 40% of healthcare-associated infection [6]. The impact of long-term central line catheters on self-inflicting harmful behaviors, such as factitious disorders, is difficult to quantitate, and recognition of these disorders remains an ongoing challenge for healthcare providers.

Case report

We present a 32-year-old Caucasian female with a past medical history of pseudotumor cerebri (ventriculoperitoneal shunt in place) and morbid obesity managed with Roux-en-Y gastric bypass. Two years after gastric bypass, necrosis of the distal pouch, stomach, and duodenum occurred, necessitating surgical debridement with abdominal reconstruction. She subsequently developed chronic malnutrition and short gut syndrome requiring long-term total parenteral nutrition through a peripherally inserted central catheter (PICC). Due to ongoing chronic pancreatitis, a pancreatic-auto-islet cell transplant with splenectomy was performed.

Five months following the pancreatic-auto-islet cell transplant, she was hospitalized three times during the same month with fever and abdominal pain. Hospitalization one Fevers were documented up to 101.2°F with a mild leukocytosis (11,400 cells/mm3). Blood cultures were positive for α-hemolytic Streptococcus (Table 1). The PICC line was removed and replaced before discharge. Hospitalization two Fevers were documented up to 100.8°F with a leukocytosis of 21,000 cells/mm3. Blood cultures were negative. Computed tomography (CT) imaging of the abdomen and pelvis did not demonstrate a source for the fever or leukocytosis. Nutritional support was maintained through enteric tube feeds, and at the patient’s preference a PICC line was again replaced for daily fluid infusion. Hospitalization three Fevers were documented up to 103°F for 3 days, with a leukocytosis of 14,300 cells/mm3. Blood cultures from the PICC line and peripheral draw grew α-hemolytic Streptococcus and Achromobacter spp. on two consecutive days. No fluid collections or intra-abdominal abscesses were found on CT imaging of the abdomen and pelvis. A chest radiograph and transthoracic echocardiogram were normal. The α-hemolytic Streptococcus and Achromobacter spp. (Table 1) were treated with 14 days of piperacillin–tazobactam.

Table 1 Microbiologic data

In clinic, following the third hospitalization, this patient reported daily fevers up to 104°F that started 1 day after being discharged from the hospital (while on piperacillin–tazobactam). She reported head and neck pain with a sore throat, which increased in severity during the febrile episodes. Mild fever of 100.9°F was present. Physical exam was normal, including the oropharynx and skin exit site of the PICC line. Outpatient workup included blood cultures, viral studies, and fungal blood tests (all were negative) (Table 1). High-resolution chest CT revealed extensive tree-in-bud infiltrates (Figure 1). The following day she reported high fevers and was admitted to the hospital for an expedited work up.

Figure 1
figure 1

High resolution chest computed tomography scan. Centrilobular nodules in the tree-in-bud configuration.

During hospitalization four there were no documented fevers. Bronchoalveolar lavage was non-diagnostic with negative cultures and cytology. The morning of hospital day five, the patient developed acute chest pain, dyspnea, mild hypotension, and hypoxia. Intravenous fluid and oxygen supplementation were administered. Echocardiogram showed new marked right ventricular dilatation with severe right ventricular dysfunction. Due to concerns for pulmonary emboli (PE), intravenous heparin therapy was initiated. CT pulmonary angiogram was negative for PE. That afternoon she was found unresponsive in pulseless electrical activity arrest. The patient died despite extensive resuscitation efforts. Mycobacterium mucogenicum eventually grew from the PICC line culture drawn from hospital day one. The cause of death at autopsy was attributed to complications from pulmonary microcrystalline cellulose emboli with associated foreign body granulomatosis (Figure 2).

Figure 2
figure 2

a Microcrystalline cellulose embolization affecting arterioles (arrowhead) and medium-sized pulmonary arteries (top-center) with associated perivascular granulomatous reaction consisting of multi-nucleated giant cells (long arrow) and epithelioid histiocytes (double long arrow) (Hematoxylin & Eosin, original magnification ×100). b Microcrystalline cellulose fibers stained salmon pink (Congo red, original magnification ×400). c Microcrystalline cellulose fibers stained gray-black with Gomori methenamine-silver (original magnification ×400). d Microcrystalline cellulose stained magenta with PAS (periodic Acid-Schiff stain, original magnification ×400).


This case demonstrates the challenge of recognizing factitious disorders in complicated medical patients with chronic conditions. The FUO with recurrent bacteremia due to atypical pathogens likely resulted from self-administration of oral medications through the center catheter, which ultimately led to a fatal pulmonary complication of microcrystalline cellulose and foreign body granulomatosis.

Recurrent polymicrobial bacteremia with an unknown source must raise suspicion of self-inflicted illness. Our patient was asplenic with a history of multiple abdominal surgeries and pancreatic-auto-islet transplant. There were many legitimate reasons to have an organic cause of fevers for which she was extensively evaluated. However, it was not until autopsy that it became clear that our patient was self-injecting oral medications through the central catheter.

Both malingering syndrome and factitious disorders misdirect practitioners, often resulting in exhaustive medical evaluations to identify organic causes of the fever. The motivating factors (either primary or secondary gain) distinguish the two conditions. Adult patients are more sophisticated in masking medical conditions, and often involve subjects with some medical background. In a 10-year review of 41 patients with factitious disorders, 39 were female and 28 held medical jobs. Once confronted with evidence that their symptoms were self-induced, many illnesses resolved or improved (17/33 cases) [4]. The mortality rate from factitious disorders ranges from 2 to 20% in small case series, [79] but is likely underrepresented and under diagnosed.

In this case, the isolation of atypical organisms, (α-hemolytic Streptococcus, M. mucogenicum, and Achromobacter spp.) is consistent with administration of unsterile solutions through the central line. Alpha-hemolytic Streptococcus is a commensal organism found in the oral flora. M. mucogenicum and Achromobacter spp. naturally reside in water and soil. M. mucogenicum is a rapidly growing mycobacterium with a highly mucoid character on solid agar [10], which may contribute to the pathogenesis of catheter infections [11]. In a large series of rapidly growing mycobacteria infections, M. mucogenicum represented the most common cause of catheter and bloodstream infections (24 of 46 cases) among a population of cancer and immunocompromised patients [12]. Bloodstream infection with M. mucogenicum has been associated with dialysis catheters, and water-borne central line infections [13, 14]. Kline et al., from our hospital, reported an outbreak of M. mucogenicum associated catheter infections from hospital and clinic tap water that contaminated the catheters during routine care and bathing [15].

Achromobacter spp. is considered an emerging pathogen in catheter related infections, and has been reported with contaminated dialysis fluid, chlorhexidine solutions, and mechanical ventilators [16, 17]. Two large series of Achromobacter spp. bloodstream infections have been published. In a cohort of cancer patients, 47 episodes of Achromobacter spp. bacteremia were characterized. Twenty-five percent were catheter associated, and 33% were nosocomially acquired [18]. Gomez-Cerezo et al. described 54 cases of Achromobacter spp. bacteremia over 10 years, in which 65% were considered catheter-related. During that time, an epidemic outbreak occurred in the hemodialysis unit. Transmission was thought to occur from healthcare workers hands after washing with contaminated hospital water [19].

Ultimately, our patient died from extensive pulmonary granulomatosis caused by the deposition of microcrystalline cellulose in the pulmonary tree with non-thrombotic pulmonary emboli (NTPE), right-sided heart failure, and sudden cardiac arrest. Microcrystalline cellulose is an inactive component commonly used as filler for oral medications including methadone and hydromorphone. With inappropriate intravenous administration, the crushed insoluble component of the oral medication (microcrystalline cellulose in our case) becomes trapped in the pulmonary arterioles causing an inflammatory cascade, thrombosis, and formation of granulomas [20]. Widespread pulmonary granulomatosis has been described in long term intravenous drug abusers, [20] and patients with factitious disorders [21]. Intravenous administration of illicit drugs, or drugs intended for oral administration, have been linked to foreign body-related NTPE [22, 23]. Foreign body embolization to pulmonary circulation can remain asymptomatic for years [24] or can be acutely fatal as demonstrated in our patient. The incidence of fatal NTPE related to intravenous administration of oral medication might be higher than reported, since diagnosis is often made on post mortem examination.

The fevers that occurred in our patient were factitious. Our patient first learned to crush her pills to administer them through the gastric-jejunal tube. In hindsight, it is logical that our patient later began to administer her oral crushed medications through the central catheter in an attempt to manage her chronic pain.


Polymicrobial and recurrent bacteremia with unusual organisms in the setting of long term indwelling central lines must alert physicians to consider self-injection of unsterile materials and factitious disorders. Recognition of these conditions becomes even more difficult in patients with complex medical conditions. In the modern era of medicine, where care may be fragmented with lack of continuity, the diagnosis of factitious syndromes and misuse of central lines are even more challenging. As this case demonstrates, factitious disorders can be fatal. It is essential that health care providers maintain a high index of suspicion of self-harming behaviors so that these syndromes can be recognized early. A multidisciplinary team approach can implement care plans to improve the outcome in these patients.



computerized tomography


fever of unknown origin


non-thrombotic pulmonary emboli


peripherally inserted central catheter


  1. Mourad O, Palda V, Detsky AS (2003) A comprehensive evidence-based approach to fever of unknown origin. Arch Intern Med 163:545–551

    Article  PubMed  Google Scholar 

  2. de Kleijn EM, Vandenbroucke JP, van der Meer JW (1997) Fever of unknown origin (FUO). I A. prospective multicenter study of 167 patients with FUO, using fixed epidemiologic entry criteria. The Netherlands FUO Study Group. Medicine (Baltimore) 76:392–400

    Article  CAS  Google Scholar 

  3. Aduan RP, Fauci AS, Dale DC, Herzberg JH, Wolff SM (1979) Factitious fever and self-induced infection: a report of 32 cases and review of the literature. Ann Intern Med 90:230–242

    Article  CAS  PubMed  Google Scholar 

  4. Reich P, Gottfried LA (1983) Factitious disorders in a teaching hospital. Ann Intern Med 99:240–247

    Article  CAS  PubMed  Google Scholar 

  5. Blyth CC, Russell S, Zwi KJ, Taitz J, Fairley M, Post JJ (2007) Munchausen syndrome by proxy and recurrent polymicrobial bacteremia. Pediatr Infect Dis J 26:191

    Article  PubMed  Google Scholar 

  6. Sievert DM, Ricks P, Edwards JR, Schneider A, Patel J, Srinivasan A et al (2013) Antimicrobial-resistant pathogens associated with healthcare-associated infections: summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2009–2010. Infect Control Hosp Epidemiol 34:1–14

    Article  PubMed  Google Scholar 

  7. Eisendrath SJ, McNiel DE (2004) Factitious physical disorders, litigation, and mortality. Psychosomatics 45:350–353

    Article  PubMed  Google Scholar 

  8. Pope HG Jr, Jonas JM, Jones B (1982) Factitious psychosis: phenomenology, family history, and long-term outcome of nine patients. Am J Psychiatry 139:1480–1483

    Article  PubMed  Google Scholar 

  9. Krahn LE, Li H, O’Connor MK (2003) Patients who strive to be ill: factitious disorder with physical symptoms. Am J Psychiatry 160:1163–1168

    Article  PubMed  Google Scholar 

  10. Springer B, Bottger EC, Kirschner P, Wallace RJ Jr (1995) Phylogeny of the Mycobacterium chelonae-like organism based on partial sequencing of the 16S rRNA gene and proposal of Mycobacterium mucogenicum sp. nov. Int J Syst Bacteriol 45:262–267

    Article  CAS  PubMed  Google Scholar 

  11. El Helou G, Viola GM, Hachem R, Han XY, Raad II (2013) Rapidly growing mycobacterial bloodstream infections. Lancet Infect Dis 13:166–174

    Article  PubMed  Google Scholar 

  12. Han XY, De I, Jacobson KL (2007) Rapidly growing mycobacteria: clinical and microbiologic studies of 115 cases. Am J Clin Pathol 128:612–621

    Article  PubMed  Google Scholar 

  13. Marshall C, Samuel J, Galloway A, Pedler S (2008) Mycobacterium mucogenicum from the Hickman line of an immunocompromised patient. J Clin Pathol 61:140–141

    Article  CAS  PubMed  Google Scholar 

  14. Fleming GA, Frangoul H, Dermody TS, Halasa N (2006) A cord blood transplant recipient with Mycobacterium mucogenicum central venous catheter infection after infusion of tap water. Pediatr Infect Dis J 25:567–569

    Article  PubMed  Google Scholar 

  15. Kline S, Cameron S, Streifel A, Yakrus MA, Kairis F, Peacock K et al (2004) An outbreak of bacteremias associated with Mycobacterium mucogenicum in a hospital water supply. Infect Control Hosp Epidemiol 25:1042–1049

    Article  PubMed  Google Scholar 

  16. Molina-Cabrillana J, Santana-Reyes C, Gonzalez-Garcia A, Bordes-Benitez A, Horcajada I (2007) Outbreak of Achromobacter xylosoxidans pseudobacteremia in a neonatal care unit related to contaminated chlorhexidine solution. Eur J Clin Microbiol Infect Dis 26:435–437

    Article  CAS  PubMed  Google Scholar 

  17. Tena D, Carranza R, Barbera JR, Valdezate S, Garrancho JM, Arranz M et al (2005) Outbreak of long-term intravascular catheter-related bacteremia due to Achromobacter xylosoxidans subspecies xylosoxidans in a hemodialysis unit. Eur J Clin Microbiol Infect Dis 24:727–732

    Article  CAS  PubMed  Google Scholar 

  18. Aisenberg G, Rolston KV, Safdar A (2004) Bacteremia caused by Achromobacter and Alcaligenes species in 46 patients with cancer (1989–2003). Cancer 101:2134–2140

    Article  PubMed  Google Scholar 

  19. Gomez-Cerezo J, Suarez I, Rios JJ, Pena P, Garcia de Miguel MJ, de Jose M et al (2003) Achromobacter xylosoxidans bacteremia: a 10-year analysis of 54 cases. Eur J Clin Microbiol Infect Dis 22:360–363

    Article  CAS  PubMed  Google Scholar 

  20. Dettmeyer RB, Verhoff MA, Bruckel B, Walter D (2010) Widespread pulmonary granulomatosis following long time intravenous drug abuse—a case report. Forensic Sci Int 197:e27–30

    Article  CAS  PubMed  Google Scholar 

  21. Mouchantaf FG, Campagna AC, Lamb CR (2011) Foreign body granulomatosis in a patient with a factitious disorder. J Bronchology Interv Pulmonol 18:179–180

    Article  PubMed  Google Scholar 

  22. Khanna D, Drehmer TJ (2001) Intravenous drug abuse mimicking vasculitis. South Med J 94:505–507

    Article  CAS  PubMed  Google Scholar 

  23. Butch AJ, Yokel RA, Sigell LT, Hanenson IB, Nelson ED (1979) Abuse and pulmonary complications of injecting pentazocine and tripelennamine tablets. Clin Toxicol 14:301–306

    Article  CAS  PubMed  Google Scholar 

  24. Thanigaraj S, Panneerselvam A, Yanos J (2000) Retrieval of an IV catheter fragment from the pulmonary artery 11 years after embolization. Chest 117:1209–1211

    Article  CAS  PubMed  Google Scholar 

Download references

Authors’ contributions

YK, JM and JG conceived the study, participated in the data collection and drafted the manuscript. RK participated in the data collection, obtained the consent and helped to draft the manuscript. CC prepared the pathology image and helped to draft the manuscript. All authors read and approved the final manuscript.


We are grateful for the contributions from the following mentors: Dr. Jo-Anne Young (editing), Dr. Bache (project assistance), Dr. Khalid Amin and Dr. Jon Ritter (pathologic diagnosis).

Compliance with ethical guidelines

Competing interests The authors declare that they have no competing interests.

Consent Written informed consent was obtained from the next of kin of the patient for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Jaime S Green.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kwon, Y., Koene, R.J., Cross, C. et al. Fatal non-thrombotic pulmonary embolization in a patient with undiagnosed factitious disorder. BMC Res Notes 8, 302 (2015).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: