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Revista da Sociedade Brasileira de Medicina Tropical

Print version ISSN 0037-8682

Rev. Soc. Bras. Med. Trop. vol.44 no.5 Uberaba Sept./Oct. 2011

http://dx.doi.org/10.1590/S0037-86822011000500025 

CASE REPORT RELATO DE CASO

 

Bacillary angiomatosis in HIV-positive patient from Northeastern Brazil: a case report

 

Angiomatose bacilar em paciente HIV positivo no nordeste brasileiro: relato de caso

 

 

Renata Félix da JustaI; Adriana Banhos CarneiroI; Jorge Luiz Nobre RodriguesI; Andréia CavalcanteI; Evelyne Santana GirãoI; Paulo Sergio SilvaI; José Telmo Valença JúniorII; Dalgimar Beserra de MenezesII; Terezinha do Menino Jesus Silva LeitãoI

IDepartamento de Saúde Comunitária, Hospital Universitário Walter Cantídio, Universidade Federal do Ceará, Fortaleza, CE
IIDepartamento de Patologia e Medicina Legal, Universidade Federal do Ceará, Fortaleza, CE

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ABSTRACT

It is a report of disseminated bacillary angiomatosis (BA) in a 23-year-old female patient, who is HIV-positive and with fever, weight loss, hepatomegaly, ascites, and papular-nodular skin lesions. The clinical and diagnostic aspects involved in the case were discussed. Bacillary angiomatosis must always be considered in the diagnosis of febrile cutaneous manifestations in AIDS.

Keywords: Angiomatosis. AIDS. Bartonella.


RESUMO

Relato de angiomatose bacilar (AB) disseminada em paciente do sexo feminino de 23 anos, HIV positiva, com febre, emagrecimento, hepatomegalia, ascite e lesões de pele pápulo-nodulares. Foram discutidos os aspectos clínicos e diagnósticos envolvidos no caso. Angiomatose bacilar deve sempre ser considerada no diagnóstico de doença febril com manifestações cutâneas na AIDS.

Palavras-chaves: Angiomatose. AIDS. Bartonella.


 

 

INTRODUCTION

Bacillary angiomatosis (BA) is an infectious disease caused by a facultative intracellular gram-negative mobile bacillus from the genus Bartonella and order Rickettsiales1. It has a worldwide distribution, and based on a recent review, Bartonella largely circulates among the Brazilian population2, with a prevalence of 1.42/1,000 AIDS patients in Rio de Janeiro, Brazil3. Commonly described in AIDS patient, BA has rarely been reported in immunocompetent individuals4 or non-HIV-infected immunosupressed patients5.

The genus Bartonella includes more than 13 species determining several syndromes in humans2. The most frequently observed are: cat-scratch disease caused by B. henselae, Carrion's disease and Peruvian wart by B. bacilliformis, trench fever by B. quintana, endocarditis and neuroretinitis by B. elizabethae, and bacillary angiomatosis and peliosis hepatis by B. henselae and B. quintana6.

Cats are the main host of B. henselae, suffering bacteremia without evidence of disease and transmitting the agent to human through bites, scratches, or fleas2; differently, B. quintana has man as the main reservoir, and it is transmitted to others by human lice2, 4.

Bacillary angiomatosis denomination comes from the vascular proliferative histopathology of skin, lymph nodes, viscera, and bones3. Therefore, the organisms can be identified in the tissues by means of silver staining when more advanced methods are unavailable3.

In Brazil, in 2001, 13 cases of BA were described in Rio de Janeiro3 and one in São Paulo7; in the following years, three more cases were reported in Sao Paulo5, 8-9. This study reports a BA case in the State of Ceará and reviews the literature concerning this disease, with emphasis in Brazilian reports.

 

CASE REPORT

An illicit drug user (crack) 23-year-old woman, born and resident in the State of Ceará in the Northeast of Brazil, known to be HIV-positive since 2004, and in irregular use of antiretrovirals therapy was admitted to the Hospital Universitário Walter Cantídio in July 2005. She had been complaining of bloody and watery diarrhea during the previous month, which worsened 3 days before her admission to the hospital. She also had been on daily fever (38ºC), abdominal pain, vomiting, anorexia, malaise, weight loss of 25kg in 9 months, dyspnea on exertion, lower extremity swelling, and painless skin lesions without précising the time they appeared.

At the time of hospital admission, she was febrile (39ºC), pale, dehydrated, malnourished (weighing 37kg) but mentally oriented, and exhibiting widespread alopecia. Candidiasis was observed on palate; the skin was dry with non-pruritic, painless erythematous papules on the face, trunk, and limbs (Figure 1). The abdomen was distended due to ascitis, with painful hepatomegaly of 4 inches below the right costal margin, but no enlarged spleen was detected; she also had moderate lower limbs edema. The CD4 count was 440 cell/mm3 less than 1 month before.

 

 

Intravenous fluid therapy and trimethoprim-sulfamethoxazole, plus anti-parasitic drug and loperamide, were started, and despite of a clinical improvement in the first week of hospitalization, anorexia, malaise, and abdominal pain persisted. In the second week, the patient´s clinical status deteriorated with dyspnea at rest and bilateral pleural effusion on chest X-ray; the liver had increased to 6cm below the costal margin. Fever persisted in irregular spikes, the skin lesions increased in number and size consisting of erythematous papules and nodules on limbs and trunk (Figure 2), and some of the lesions progressed to ulceration.

 

 

Smear and culture from bone marrow aspiration were negative for histoplasmosis, tuberculosis, and leishmaniasis (smear only). Hepatitis B and C virus serologies were also negative; the myelogram displayed dysmyelopoiesis with mild plasmocytosis, and the abdominal ultrasound showed moderate hepatomegaly and ascites. The serum enzymes - aspartate aminotransferase (AST) and alanine aminotranferase (ALT) - were on the normal range, and the gamma-glutamyltransferase - GGT (329U/L) - and alkaline phosphatase - ALP (796U/L) - were higher.

In the third week, the patient presented low blood pressure (90x50mmHg), tachycardia (132 beats/minute), and persistent fever. Further increase was noted in the liver size, (8cm below the costal margin) and in the number of erythematous papules with spontaneous bleeding in a few. Blood cultures isolated Staphylococcus aureus sensitive to vancomycin, and clinical improvements were observed after initiation of the sepsis treatment.

The following abdominal ultrasonography showed enlarged liver associated to signs of diffused parenchymal disease without nodules, with normal vessels. Lymphonodes were found in the peripancreatic, perihilar, and retroperitoneal regions, as well as moderate ascites and slight enlargement of the spleen.

Histopathological examination of skin lesions by shaving disclosed vascular proliferation of capillaries with typical endothelial cells, accompanied by edema, neutrophils, and basophils packed with clumps of bacilli visible at Grocott stain, consistent with the diagnosis of bacillary angiomatosis. Therapy was initiated with erythromycin (500mg orally, four times a day) and gentamicin (1.7mg/kg IV 8/8 h), with gradual improvement, disappearance of fever, and normalization of vital signs and laboratorial parameters. The patient was discharged on the use of highly active antiretroviral therapy and erythromycin scheduled for 4 months.

 

DISCUSSÃO

Bacillary angiomatosis is a systemic disease with frequent cutaneous involvement4, 9. These manifestations occur as angiomatous papules or nodules of different sizes affecting different areas of the body surface, with erythematous, wine-like, or skin color lesions, with smooth or crusty aspect, which can be single or multiple, compressible, tense, or friable. Regional lymphadenopathy can occur, and it is often painful1, 4, 8-9.

Bacillary angiomatosis may be accompanied by disseminated visceral involvement as the one described in the current report1. The tissues involved are bone, brain, lymph nodes, respiratory and gastrointestinal tracts, liver, and spleen1. There may also be fever, anorexia, weight loss, abdominal pain, nausea, vomiting, and diarrhea, especially when there is visceral involvement, primarily liver and spleen, as in this case report1, 4.

Internal involvement, especially of the liver, spleen, and bone marrow, can be manifested with or without peliosis. Bacillary peliosis is characterized by vascular dilatation and hemorrhagic cystic spaces surrounded by fibromyxoid stroma. Generalized hepatomegaly, focal hepatic abscesses, and granulomatous hepatitis represent forms of hepatic pathology that have been associated with B. henselae infection9. High levels of alkaline phosphatase are also frequently found in BA cases1, 3, 9.

The hepatic ultrasound of the current patient did not present any vascular abnormalities; however, it showed increased ALP and GGT enzymes.

Bacillary angiomatosis affects most commonly the HIV-positive patients when compared with other types of immunodeficiency; the majority is seen1, 3 in advanced stage of AIDS and CD4 count less than 200 cells/mm3. The patient presented here had a CD4 count of 440 cells/mm3, which is not commonly observed; therefore, other factors must have contributed to the development of this disease, like poor living conditions.

All cases previously reported in Brazil3, 5, 7-9 were in HIV-positive patients, except one5. A case was reported from São Paulo in 20017: a 41-year-old male patient had skin lesions predominantly ulcerated and bleeding, weight loss, and bone lesions. In the same year, 13 cases of BA were described in Rio de Janeiro3. Among these, 10 (76.9%) patients had cutaneous or subcutaneous lesions, 11 (84.6%) had fever, nine (69.2%) had weight loss, eight (61.5%) had hepatomegaly, seven (53.8%) had diarrhea, and two (15.4%) complained of bone pain.

The Brazilian case reported in a non-HIV-infected immuno-supressed patient was in a 15-year-old renal-transplanted male. This patient complained of a painful reddish tumor in the cervical region, which increased progressively in a month and was associated to high fever, enlarged abdominal lymphnodes, and hepatosplenomegaly5.

A case of a 49-year-old female patient who presented papular and papular-nodular painful bleeding lesions, associated to fever and weight loss8, was reported in Campinas, State of São Paulo, Brazil in 2006. In the following year, another case was reported in the same city: a 36-year-old male patient, an illicit drug user and presenting fever, progressive abdominal distension by ascites, hepatosplenomegaly, and weight loss9. A pedunculated tumor in the perineal region with irregular surface and erythematous base was observed as well as numerous small angiomatous papules all over the body. He also had anemia and CD4 count of 15 cells/mm3.

Although BA is more prevalent in males (90% of cases), the present report describes the case of a female patient. Diagnosis can be easily made by histological examination of skin lesions, mainly when electron microscopy is unavailable. Polymerase chain reaction, serology (indirect immunofluorescence tests and ELISA for B. henselae and B. quintana), and, less commonly, blood and tissue cultures can also be carried out4, 8.

Differential diagnoses of bacillary angiomatosis include Kaposi's sarcoma (that can coexist in the same patient), pyogenic granuloma, Peruvian wart, cutaneous T-cell lymphoma, Hodgkin and non-Hodgkin's lymphomas, atypical mycobacterial infection, and disseminated histoplasmosis4. Special attention must be given to disseminated histoplasmosis in the State of Ceará, based on the high frequency of this disease in that setting10.

The most efficient treatment consists of erythromycin, 500mg four times a day for 8 to 16 weeks, or doxycycline, two times a day for 8 to 16 weeks. A second option consists of clarithromycin, 500mg, and azithromycin, 250mg, twice a day4.

Bartonella infection offers a good response to antibiotics and has to be taken into account in the investigation of febrile cutaneous manifestations in AIDS. The skin lesion and the histopathological study can easily define the diagnosis.

 

REFERENCES

1 Velho PENF, Souza EM, Cintra ML, Mariotto A, Moraes AM. Bacillary angiomatosis: literature review and iconographic documentation. An Bras Dermatol 2003; 78:601-609.         [ Links ]

2. Lamas C, Curi A, Bóia MN, Lemos ERS. Human bartonellosis: seroepidemiological and clinical features with an emphasis on data from Brazil. A Review. Mem Inst Oswaldo Cruz 2008; 103:221-235.         [ Links ]

3 Gazineo JLD, Trope BM, Maceira JP, May SB, Coelho JMCO, Lambert JS, et al. Bacillary angiomatosis: description of 13 cases reported in five reference centers for AIDS treatment in Rio de Janeiro, Brazil. Rev Inst Med Trop S Paulo 2001; 43:1-6.         [ Links ]

4 Faria AL, Carvalho R, Lima N. Angiomatose bacilar em doente imunocompetente: a propósito de um caso clínico. Arq Med 2008; 22:17-19.         [ Links ]

5 Belangero VMS, Tresoldi AT, Prates LC, Mendes RP, Catherino P, Rigatto SZP, et al. Bacillary Angiomatosis After Kidney Transplantation. J Bras Nefrol 2006; 28:168-70.         [ Links ]

6 Vasquez TP, Chanqueo CL, García CP, Poggi MH, Ferrés GM, Bustos MM, et al. Angiomatosis bacilar por Bartonella quintana en un paciente con infección por virus de inmunodeficiencia humana. Rev Chil Infectol 2007; 24:155-159.         [ Links ]

7 Barra LAC, Tranchitella FB, Suleiman JMAH, Bedaque EA, Martinelli FLB, Xavier MC, et al. Bone lesions due to bacillary angiomatosis: case report and literature review. Rev Bras Ortop 2001; 36:401-405.         [ Links ]

8 Velho P, Souza EM, Cintra ML, Moraes AM, Tanaka AMU. Diagnóstico da infecção por Bartonella spp.: a propósito de um caso de angiomatose bacilar. An Bras Dermatol 2006; 81:349-353.         [ Links ]

9 Velho PE, Pimentel V, Del Negro GM, Okay TS, Diniz PP, Breitschwerdt EB. Severe anemia, panserositis, and cryptogenic hepatitis in an HIV patient infected with Bartonella henselae. Ultrastruct Pathol 2007; 31:373-377.         [ Links ]

10 Pontes LB, Leitão TMJS, Lima GG, Gerhard ES, Fernandes TA. Clinical and evolutionary characteristics of 134 patients with disseminated histoplasmosis associated with AIDS in the State of Ceará. Rev Soc Bras Med Trop 2010; 43:27-31.         [ Links ]

 

 

Address to:
Dra. Terezinha do Menino Jesus Silva Leitão.
Deptº Saúde Comunitária/UFC. Rua Prof. Costa Mendes 1608/5° andar
Rodolfo Teófilo, 60430-140 Fortaleza, CE, Brasil.
Phone: 55 85 3366-8044
e-mail: tsilva@ufc.br

Received in 20/09/2010
Accepted in 19/04/2011