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versión impresa ISSN 0120-4157

Biomédica vol.37 no.3 Bogotá jul./set. 2017 


Toxoplasmosis diseminada en un paciente con trasplante de corazón a pesar de la profilaxis con trimetoprim-sulfametoxazol

Disseminated toxoplasmosis in a heart transplant patient despite cotrimoxazole prophylaxis: A case report

Victoria Dávila1  , Gustavo Roncancio-Villamil1  2  , Luis Alfonso Correa3  4  , Catalina Restrepo4  , Camilo Alberto Madrid1  , Javier Mauricio González1 

1Servicio de Enfermedades Infecciosas, Clínica Cardio VID, Medellín, Colombia

2Escuela de Ciencias de la Salud, Universidad Pontificia Bolivariana, Medellín, Colombia

3Servicio de Patología, Laboratorio Clínico VID, Medellín, Colombia

4Sección de Dermatología, Departamento de Medicina Interna, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia


Se reporta el caso de un paciente de sexo masculino, de 61 años de edad, quien ocho meses después de someterse a un trasplante de corazón presentó una enfermedad sistémica con compromiso del sistema nervioso central y del sistema inmunológico, así como de pulmón, riñón, colon y piel, y a quien finalmente se le diagnosticó toxoplasmosis diseminada, a pesar de haber recibido profilaxis con trimetoprim-sulfametoxazol, debido a que el órgano provenía de un donante positivo para toxoplasmosis siendo él un receptor negativo. Se discuten las opciones de profilaxis en nuestro medio.

Palabras-clave: toxoplasmosis; trasplante de corazón; tolerancia inmunológica; seroconversión


We report the case of a 61 year-old male who underwent heart transplantation eight months before developing a systemic condition with central nervous system, lung, kidney, colonic, cutaneous, and hematologic involvement, found to be secondary to a systemic toxoplasmosis despite co-trimoxazole prophylaxis in a previous-to-transplant seronegative patient receiving a heart from a seropositive donor. A review of prophylactic options in our environment is discussed.

Key words: Toxoplasmosis; heart transplantation; immune tolerance; seroconversion

Toxoplasmosis is an infection caused by the protozoonToxoplasma gondii. Itis prevalent worldwide, affectingapproximately one third of the world's population (1). Seroprevalence increases with age and there is no genderdifference.

Toxoplasmosis is transmitted via oral intake of food contaminated with the parasite's cysts or oocysts. However, there are reports of transmission throughtransplanted organs and blood transfusions, as well as vertical transmission (2).

It evolves to a systemic disease, and only 10% of theaffected population is symptomatic. The clinical course is usuallybenign, but it can be lethal, especially in immunosuppressed patients (3). Systemic clinical signs include generalizedadenopathies, myocarditis, polymyositis, pneumonitis, encephalitis and chorioretinitis. Skin manifestations are rare, though usually present in immunosuppressed patients. Giventhe great variability in the appearance of cutaneous toxoplasmosis, histopathological studies are required for diagnosis.

Although direct observation of the parasite is possible in most tissue samples, diagnosis should be confirmed by immunohistochemistry and polymerase chain reaction (PCR) (4).

Medical therapy is indicated when there is active skin or ocular infection, or congenital disease, and in all immunosuppressedpatients. Sulfadiazine in combination with pyrimethamine is the treatment of choice. Seronegative heart transplant patients shouldreceive prophylaxis with pyrimethamine and sulfadiazine for the first three months followed by co-trimoxazole for the rest of their lives (5,6).

Case report

We report the case of a 61-year-old male patient with a past medical history of hypertension, dyslipidemia, hypothyroidism, heart failure with preserved ejection fraction and severe coronary artery disease, in whom surgical and percutaneous revascularization were performed. After surgery, the patient developed refractory angina despite optimal anti-ischemic medication which led to heart transplantation. Laboratory tests previous to transplant were discordant for T. gondii and human herpes viruses type I and II. The donor had positive immunoglobulin M(IgM), negative immunoglobulin G (IgG) for T. gondii,and positive IgG for herpes viruses (HV) type I and type II. The receptor was negative for both.

After eight months of transplant the patient was admitted with persistent diarrhea lasting 20 days, abdominal pain and malaise. The immunosuppression regimen included mycophenolate mofetil, 1 g every 12 hours, prednisolone, 5 mg per day, and cyclosporine, 150 mg every 12 hours. Prophylaxis with co-trimoxazole, 160/800mg per day, wasalso given.

On physical examination the patient presented withtachycardia, normal blood pressure and respiratory rate, and nofever was documented. Vesicular lesions with clear content and erythematous base with dermatome distribution wereseen in the right gluteus.

Initial laboratory tests showed anemia, leukopenia with lymphopenia, renal dysfunction and a positive Tzank test (table 1). Viral load for cytomegalovirus (CMV) was positive with 404.000 copies/ml; therapy with ganciclovir, 5 mg/kg every 12 hours, was started with initial improvement of the diarrhea.

Table 1 Diagnostic aids 

However, two weeks later the patient persisted with leukopenia, the anemia worsened requiring red blood cell (RBC) transfusion and he developed fever as high as 39.8º C. The only additional finding was four 5 mm to 1 cm erythematous, mildly painful lesions, some in legs and thighs with white scaling in the center, and a similar lesion in the upper right eyelid (figure 1). The diarrhea reappeared, renal dysfunction worsened, as well as the completeblood count (CBC), now with pancytopenia (anemia, leukopenia, lymphocytopenia, neutropenia and thrombocytopenia).

Figure 1 A 5 mm erythematous papule with white scaling in the center 

Empirical therapy with anidulafungin plus cefepime was started for febrile neutropenia. Toxoplasma antibody seroconversion was documented. Therapy with clindamycin plus pyrimethamine wasstarted and the skin lesions were biopsied.

Histopathology of skin lesions was positive and immunohistochemistry for toxoplasmosis confirmed the presence of the parasite (figure 2 and figure 3). Molecular studies with blood and cerebrospinal fluid (CSF) PCR were also positive forToxoplasma(7). Central nervous system magnetic resonance (MR) did not show focal lesions.

Figure 2 Skin histology from the lower limb showing T. gondii tachyzoites forming a pseudocyst. Giemsa stain, 40X. 

Figure 3.Special immunohistochemical staining for toxoplasma from the skin biopsy showing a pseudocyst. Toxoplasma RB9423-P rabbit monoclonalantibodies (Thermo (r) ) were used. 

The initial course was unfavorable, the patient persisted with fever, headache, encephalopathy, oliguric renal failure, hepatitis,pancytopenia, metabolic acidosis and increased lactate dehydrogenase (LDH) up to 2.500 IU/L. Pulmonary patchy infiltrates were found. He was admitted to the intensive care unit for mechanical ventilation. Plasma exchange was started for suspected thrombotic thrombocytopenic purpura.

After a few days the patient´s status improved, especially renal function and blood counts, but he persisted with hypogammaglobulinemia. CMV infection relapsed with poor response to ganciclovir. Gammaglobulin, 30 g intravenous (IV) weekly, was started with complete remission.

He was released after six weeks of therapywith clindamycin and pyrimethamineupon suspicion of co-trimoxazoleresistance. Suppression with co-trimoxazole plus valganciclovir and gammaglobulin was maintained and the patient has been symptom-free for 28 months.


This is a heart transplant patient whodeveloped systemic toxoplasmosis with central nervous system, pulmonary, renal, colonic, cutaneous, and hematologic compromise secondary to disseminated toxoplasmosis. Toxoplasma gondii infection after heart transplant is often a severe disease. The clinicalpresentation ranges from chorioretinitis to disseminated infection (pulmonary, myocardial, hepatic and CNS infection) (8).

Toxoplasmosis in immunocompromised patients is usually secondary to a reactivation of latent infection from the donor (9). In this case, previous to transplantation the donor´s toxoplasmosis serology was discordant with the recipient´s.Toxoplasmacysts may persist in the donor's myocardium, thus, hosts are at higher risk of developing the disease. With immunosuppression, the bradyzoites become tachyzoites, quickly proliferating and consequently destroying cells.

Before the use of prophylaxis with co-trimoxazole there was a higher risk of disseminated toxoplasmosis (10). Studies of seronegative heart recipients have found that the risk of T. gondii-associated clinical disease ranges from 0 to 82% if patients receive organs from seropositive donors without antimicrobial prophylaxis (6,8).

Seronegative heart transplant patients should receive prophylaxis. Effective regimens include one single-strength co-trimoxazole tablet daily, one double-strength three times a week, 1,500 mg atovaquone daily or pyrimethamine 25 mg/day. This patient had received prophylaxis with co-trimoxazole. Results from observational studies have shownthat this drug is effective in preventingtoxoplasmosis, even in cardiac recipients (6,11).

The patient may have developed severe disease despite co-trimoxazole prophylaxis due to resistance to sulfonamide (12,13). In this sense, more-virulentToxoplasmastrains have been found in Colombia and transmissionof toxoplasmosis by renal transplant was reported in two local cases (14,15). This suggests that the risk could be higher in tropical zonesof the Americas where a high genetic diversity of Toxoplasma has been found.

Co-trimoxazole is provided as a 1/5 ratio combination of trimethoprim and sulfamethoxazole. This ratio was chosen in order to provide synergistic ratio against bacteria, but due to the poor efficacy of trimethoprim against T. gondii trophozoites (100 times lower than pyrimethamine), the optimal ratio of the two compounds against this infection is probably closer to 1/1 (16). High doses of co-trimoxazole are needed to cure experimental acute infection in mice, and relapses are observed after cessation of therapy, because it is ineffective on the cyst form of the parasite. However, it has proved remarkably efficient in the treatmentand prophylaxis of toxoplasmosis in transplant patients with AIDS (11).

Considering that a high genetic diversity, gene polymorphisms in the dihydrofolate reductase and dihydropteroate synthase genes, more-virulent strains of T. gondii,and several transplanted patients with disseminated toxoplasmosis have been reported in Colombia, the recommended doses of co-trimoxazole could be insufficient, or another agent (e.g., dapsone plus pentamidine or pyrimethamine and sulfadiazine) could be necessary to prevent toxoplasmosis in high risk transplant patients.

It is also important to point out that this patient developed symptoms after eight months of transplantation. Previous reports have described how heart transplantpatients receiving the organ from seropositive donors usually develop infections four to twelve weeks after transplantation. According to previous reports, the organs most commonly affected by systemic toxoplasmosis in immunosuppressed patients are the lungs and the central nervous system (17,18).

To our knowledge, this is the first heart transplant patient reported in the literature presenting toxoplasmosis with cutaneous manifestations. Such cutaneous involvement is quite rare, and only a few cases have been reported in immunocompromised patients with great variability in the appearance of skin lesions. Generalized rash, erythema multiform-like lesions, nodular lesions and vesicular varicella-like lesions have been described (19-21). Skin biopsies confirmed the presence of the parasite, but histopathological findings are variable. The involvement of the colon is also unique in this patient.

We can conclude, then, that diagnosing toxoplasmosis in immunosuppressed patients is challenging, as any organ may be affected. Thus, toxoplasmosis should always be suspected as a differential diagnosis in patients with systemic symptoms.Patients must be studied thoroughly, using all possible diagnostic aids to rule out the disease, including serology, histology, special immunohistochemical staining and PCR (22-23). Co-trimoxazole prophylaxis does not exclude the diagnosis and resistance studies are necessary.


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Funding No funding was received

Recibido: 15 de Diciembre de 2015; Aprobado: 20 de Octubre de 2016

Corresponding author: Gustavo E. Roncancio, Calle 78N N° 75-21, Medellín, Colombia Teléfono: (574) 445 4000, extensión 4314; fax: (574) 441 7837

Conflict of interests The authors declare no conflict of interests

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