J Korean Orthop Assoc.  2019 Feb;54(1):72-77. 10.4055/jkoa.2019.54.1.72.

Late-Onset Candida Vertebral Osteomyelitis in Two Young Patients Who Underwent Heart Transplant Surgery

Affiliations
  • 1Department of Orthopedic Surgery, Seoul Red Cross Hospital, Seoul, Korea.
  • 2Department of Orthopedic Surgery, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Korea. sthkim96@gmail.com

Abstract

Candida vertebral osteomyelitis (CVO) is a rare disease that is a complication of intravenous drug use, but recently it has been recognized as mostly an opportunistic infection. Because CVO appears to mimic pyogenic spondylodiscitis in terms of the clinical and radiologic presentations, it is often neglected in a usual clinical setting. The clinical, radiological, and biological characteristics of CVO are often used to make a differential diagnosis with vertebral osteomyelitis from other etiologies. Once an initial proper diagnosis was performed, the treatment relies on the prompt initiation of appropriate pharmacotherapy and serial monitoring of the clinical progress. This paper report late-onset CVO in two young patients who underwent a heart transplant surgery and had postoperative systemic candidiasis. These two cases are a good reminder of the potential of CVO in immunosuppressive patients treated with anti-fungal agents. This paper presents these two cases with a review of the relevant literature.

Keyword

Candida vertebral osteomyelitis; opportunistic infection; late-onset; heart transplantation

MeSH Terms

Candida*
Candidiasis
Diagnosis
Diagnosis, Differential
Discitis
Drug Therapy
Heart Transplantation
Heart*
Humans
Opportunistic Infections
Osteomyelitis*
Population Characteristics
Rare Diseases

Figure

  • Figure 1 Plane lateral radiograph (A), sagittal T2-weighted image (WI) (B), sagittal T1WI (C), and contrast-enhanced T1WI magnetic resonance imaging (D) demonstrate endplate erosion and small T2 high signal intensity change foci of L1-2 intervertebral disc, but relatively preserving the intervertebral disc integrity. On the other hand, there was no significant epidural and paravertebral soft tissue abscess formation.

  • Figure 2 Sagittal T2-weighted image (WI) (A) and sagittal T1WI magnetic resonance imaging (MRI) (B) demonstrate superior endplate erosion of L4, bone marrow edema of the inferior endplate of L3, and bone marrow edema with small abscess formation at inferior endplate corner of T12. (C) Thoracic sagittal T2WI MRI demonstrates endplate erosion with fluid at the T7-8 intervertebral disc. On the other hand, there was no significant paravertebral or epidural abscess formation.

  • Figure 3 (A) Histology findings. The photomicrographs show a granulomatous inflammation and fibrosis in the marrow space, but no microorganisms are present (H&E, ×200). (B) Polymerase chain reaction analysis revealed a positive band of fungal DNA in the biopsy of the bone marrow. Pyrosequencing analysis showed that the fungal DNA originated from Candida albicans. M, size marker; P, positive control of candida species; N, negative control; Pt, patient's sample.

  • Figure 4 (A) Histology findings. Photomicrographs show marrow fibrosis as well as an infiltration of chronic inflammatory cells, but no microorganisms can be found (H&E, ×200). (B) Polymerase chain reaction analysis revealed a positive band of fungal DNA in the biopsy of the bone marrow. Pyrosequencing analysis showed that the fungal DNA originated from Candida species. M, size marker; P, positive control of candida species; N, negative control; Pt, patient's sample.

  • Figure 5 Follow-up sagittal T2-weighted image magnetic resonance imaging demonstrate complete resolution of the intravertebral and interspace abscess without a spinal deformity in the 27-year-old male patient (A) and in the 24-year-old female patient (B).


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