Fungal chorioretinitis with systemic candidiasis in an infant following treatment with broad spectrum antibiotics: A case report.

Fungal chorioretinitis is a rare complication of neonatal fungemia that may lead to vision loss. Early diagnosis and aggressive treatment are essential to avoid vision loss. This study describes a case of a full term infant with candidiasis infection, which disseminated from the eye to the hip joint, and the diagnosis and treatment of fungal chorioretinitis and hip osteoarthritis with systemic candidiasis. The current case report indicates that the duration of therapy for fungal chorioretinitis should be at least 4-6 weeks long and should ideally continue until all clinical evidence of intraocular infection has been resolved. Close follow-up of infants who survive fungemia is essential. Therefore, early diagnosis and appropriate duration of antifungal treatment are necessary.

Introduction

Endogenous fungal chorioretinitis in newborn infants is a rare condition that may lead to vision loss (1). To the best of our knowledge, a Candida infection disseminating from the eye to the hip joint in infants has not been previously reported. Early diagnosis and aggressive treatment are essential to avoid vision loss. Ocular candidiasis is a serious complication of candidemia, but little information has been published on the optimal duration of treatment. Based mainly on expert opinion, the Infectious Diseases Society of America guidelines propose 4–6 weeks of treatment for endophthalmitis with the duration being determined by the stabilization or resolution of eye lesions (2). The current case report describes a case of successfully treated fungal chorioretinitis and hip osteoarthritis with systemic candidiasis, in a full term infant following treatment with antibiotics.

Case report

A 39-week-gestation female infant was delivered by caesarean section at The First Hospital of Jilin University (Changchun, China) in September 2014. At day 6 postpartum, the patient became febrile, with a temperature of 39°C and experienced vomiting. The patient was diagnosed with septicemia and neonatal meningitis. Following intravenous administration of cefepime (30 mg/kg) twice a day for 11 days, a prominent conjunctival infection developed in the left eye. Cultures for Candida albicans in the blood and cerebrospinal fluid tested positive. Other tests include blood tests [white blood cells 0.9×109/l (neutrophils 0.216×109/l, lymphocytes 0.684×109/l), red blood cells 5.25×1012/l, hemoglobin 189 g/l, platelet 279×109/l] and cerebrospinal fluid tests [Cl 121 mmol/l, Glu 0.8 mmol/l, protein 1.0 g/l, Pandy's test (−), white blood cells 20×106/l (macropolycytes 8×106/l, monocytes 12×106/l), red blood cells 70×106/l]. Ophthalmic examination indicated one yellow-white chorioretinal juxta foveal lesion in the left eye, with neither vitreous haze nor cells (Fig. 1). Chest X-ray and tuberculin skin test were normal. Intravenous fluconazole (6 mg/kg daily; Lunan Pharmaceutical Group Co., Ltd., Linyi, China) administration was begun instead of cefepime for the treatment of fungal infection. The patient stopped vomiting and the temperature was 36.8°C following the use of fluconazole for 20 days. Cultures for Candida albicans in the blood and cerebrospinal fluid tested negative. Subsequently, the patient was discharged.

Figure 1.

Fundus photograph of the left eye at day 17 postpartum, presenting an active chorioretinal lesion due to Candida infection.

However, 6 days after discharge, the patient was referred to The First hospital of Jilin University with a 1-day history of fever and limitation of motion in the right hip. A diagnosis of hip osteoarthritis was established by magnetic resonance imaging (Fig. 2). Fundus examination indicated that the lesion had expanded and extended to the inferior and superior temporal vascular arcades in the left eye (Fig. 3). Following a further 4 weeks of intravenous fluconazole administration (6 mg/kg daily), no active chorioretinal lesions were observed in the fundus examination (Fig. 4) and limitation of motion in the right hip was completely resolved. The blood culture for C. albicans was negative. Three months later, the patient remained asymptomatic and fundus examination was unremarkable.

Figure 2.

Magnetic resonance imaging scan, taken at day 6 after the patient was first discharged. The scan indicates the presence of hip osteoarthritis.

Figure 3.

Fundus photograph of the left eye, taken at day 6 after the patient was first discharged. The chorioretinal lesion had expanded to the inferior and superior-temporal vascular arcade.

Figure 4.

Fundus photograph of the left eye, taken after the second 4-week period of antibiotic treatment. No active chorioretinal lesion is visible.

Discussion

Fungal chorioretinitis is defined as the presence of deep, focal, white chorioretinal lesions with no evidence of direct vitreous involvement (3) and it is rarely diagnosed in newborn infants due to high availability of prophylactic antifungal therapy (1). Those at risk of developing fungal chorioretinitis include hospitalized patients with a history of a compromised immune system, diabetes mellitus, intravenous drug use, chronic use of indwelling catheters, use of broad spectrum intravenous antibiotics or hyperalimentation (4,5). The risk factor for the patient in the current study was treatment with broad spectrum antibiotics.

The most common causative species of candidemia identified in fungal culture is C. albicans (41%), followed by Candida parapsilosis (24%) and Candida glabrata (13%). The most common organ of dissemination is the lung (58%), followed by the liver (23%), kidney (16%), brain (12%), spleen (8%), heart (8%) and eye (8%) (4). The probability of fungus disseminating to a given organ seems be correlated with the relative size and blood supply of that organ (6). Of 38 heroin users treated for systemic Candida infections, 10 had osteoarticular involvement (vertebrae, costal cartilage, knees and sacroiliac) (7). To the best of our knowledge, this is the first report of Candida infection disseminating from the eye to hip joint in an infant. Ophthalmologists should be aware of this unusual complication when treating active Candida chorioretinitis.

When treating patients with fungal chorioretinitis, there is some debate over the appropriate duration of systemic antifungal therapy. According to the most updated guidelines, the duration of therapy for fungal chorioretinitis should be at least four to six weeks and should ideally continue until all clinical evidence of intraocular infection has been resolved (2). The current case is consistent with these guidelines, supporting the proposal that four weeks of antifungal treatment is necessary. Although the occurrence of ocular infection is very low in newborns, close follow-up of infants who survive fungemia remains essential, as in a minority of cases, preterm infants with successfully treated fungemia may develop a fungal abscess in the crystalline lens, as a result of Candida sequestration (8).

In conclusion, in cases of fungal chorioretinitis, early detection and rational duration of treatment using fluconazole or other systemic antifungals may prevent severe ocular involvement and avoid lifelong visual impairment. Particular care should be taken to test for fungal chorioretinitis in the presence of risk factors or external signs of intraocular inflammation (3,9,10). To the best of our knowledge, this is the first reported case of a Candida infection disseminating from the eye to the hip joint in an infant. The patient was successfully treated with fluconazole, and the current results suggest that at least four to six weeks of antifungal treatment should be administered in future cases.