Journal of Family & Community Medicine
Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contact us Login 
 

Users Online: 61 Home Print this page Email this page Small font sizeDefault font sizeIncrease font size

 

 Table of Contents 
CASE REPORT
Year : 2009  |  Volume : 16  |  Issue : 2  |  Page : 71-73  

Acute plasmodium vivax malaria presenting with pancytopenia secondary to hemophagocytic syndrome: Case report and literature review


Department of Internal Medicine, King Fahd Hospital of the University, Al-Khobar, Saudi Arabia

Date of Web Publication16-Jun-2012

Correspondence Address:
Waleed Albaker
Department of Internal Medicine, King Fahd Hospital of the University, P.O. Box 2208, Al-Khobar 31952
Saudi Arabia
Login to access the Email id

Source of Support: None, Conflict of Interest: None


PMID: 23012194

Rights and PermissionsRights and Permissions
   Abstract 

Pancytopeni,a as an initial manifestation of acute plasmodium vivax malaria is extremely rare and mainly reported with plasmodium falciparum. We report a 37- year old Nepali patient who recently came to Saudi Arabia and presented with a three-week history of intermittent fever, chills and rigor. She was found to have spleenomegaly, pancytopenia, hyperferrtinemia, and hypofibronogenemia with positive peripheral blood smear for plasmodium vivax. The patient had a full recovery from pancytopenia with oral chloroquine.

Keywords: Pancytopenia,plasmodium vivax,hemophagocytosis,malaria,bone marrow failure.


How to cite this article:
Albaker W. Acute plasmodium vivax malaria presenting with pancytopenia secondary to hemophagocytic syndrome: Case report and literature review. J Fam Community Med 2009;16:71-3

How to cite this URL:
Albaker W. Acute plasmodium vivax malaria presenting with pancytopenia secondary to hemophagocytic syndrome: Case report and literature review. J Fam Community Med [serial online] 2009 [cited 2020 Jul 10];16:71-3. Available from: http://www.jfcmonline.com/text.asp?2009/16/2/71/97001


   Introduction Top


Unlike plasmodium falciparum, Plasmodium vivax malaria is rarely associated with severe complications. One of the complications is pancytopenia, which can occur in vivax infection secondary to microangiopathic hemolytic anemia. Another mechanism of pancytopenia in vivax infection is hemophagocytic syndrome, but this is extremely rare and few cases are reported in the world literature. We report a rare case of plasmodium vivax malaria with pancytopenia, secondary to hemophagocytic syndrome. The suggested management strategy of this unique presentation is highlighted. We think that physicians in Saudi Arabia should be aware of such a presentation since there are a lot of people from endemic regions who are working and residing in the Kingdom.


   Case Report Top


A 37-year old female patient from Nepal, who recently came to Saudi Arabia as a housemaid, presented at the Emergency Department in August 2008 with fatigue, headache, intermittent fever, chills and rigor of three weeks' duration. She gave a history of several febrile illnesses in the past few years that were presumed to be malaria and treated as such, although no documentation was available. Upon presentation, she was febrile with a temperature of 39.5 ° C. She was very pale, had a palpable spleen, 5 cm below left costal margin. The rest of the physical examination was unremarkable. Her initial blood tests were remarkable for pancytopenia with WBC of 2.9 x 10 9, Neutrophils of 0.8 x 10 9 /l, platelet of 52 x 10 9 /l and hemoglobin of 5.6 g/dl. She had a normal reticulocytes count of 2% and an indirect bilurubin of 0.2 mg/dl. Her ferritin level was elevated more than 554 lg/l with Fibrinogen level of 0.8 g/L. Her initial peripheral blood smear showed ring forms, developing trophozites and mature schizonts of plasmodium vivax without any evidence of shiztocytes. She had negative serological evidence of CMV, Parvovirus B19 and hepatitis. All her septic blood and urine work up were unremarkable. Her abdominal ultrasound

confirmed an enlargement of the spleen. She was treated with oral chloroquine 300 mg/d for 5 days and her condition improved rapidly with complete resolution of her pancytopenia and plasmodium vivax [Table 1]. Bone marrow aspiration was not considered since she demonstrated quick recovery of pancytopenia following oral chloroquine on the third day of treatment. She was discharged on primiquine for 15 days to assure complete eradication of the vivax infection.
Table 1: Laboratory results before and after treatment

Click here to view



   Discussion Top


Plasmodium Vivax malaria is one of the parasitic infections transmitted by mosquitoes. It usually results in minimal complications with intermittent fever, chills and rigors following mosquito bites. Its life cycle is characterized by a hepatic phase which keeps the vivax infection in a dormant stage resulting in recurrence and relapse after treatment. [1] .We report a rare case of acute plasmodium vivax with pancytopenia secondary to hemophagocytic syndrome. Our patient had a fever, spleenomegaly, pancytopenia, hyperferritinemia and hypofibrinogenemia which are consistent with hemophagocytic syndrome based on the recent revised criteria 2007 [Table 2]. [1] This criteria did not mandate bone marrow aspiration for diagnosis.
Table 2 : Diagnostic criteria for hemophagocytic syndrome1

Click here to view


Hemophagocytic syndrome (HPS) is probably due to inappropriate or excessive immunologic responses of T cells .In HPS, high levels of IFN-gamma, soluble IL-2 receptor, TNF-a, IL-1, and IL-6 have been demonstrated, suggesting that elaboration of activating cytokines by T-helper cells promotes activation of macrophages in this disease .These cytokines depress the proliferation of progenitor cells, which aggravate the pancytopenia as a result of phagocytosis of the blood cells .This has been attributed secondary to different infections including Viral (e.g. EBV, CMV, Varicella) Bacterial (e.g. Gram-negative rods, Pneumococcus, Mycoplasma pneumonia) Fungal (e.g. Candida albicans, Cryptococcus neoformans, Histoplasma capsulatum) and Parasitic (e.g. Babesia microti , Plasmodium falciparum, Strongyloides stercoralis ). [2]-[4] A recent report from India revealed that pancytopenia is a completely atypical manifestation of plasmodium vivax which occurs in only 0.9 %. [5]

HPS secondary to plasmodium vivax is rarely reported in the literature. To our knowledge, there are four reported cases of plasmodium vivax with pancytopenia. [4],[5],[6],[7],[8] Three cases had isolated vivax infection and one had combined vivax and falciparum infection.

Fortunately, we were able to detect the plasmodium vivax on the peripheral blood smear upon presentation. Chloroquine was started immediately resulting in quick recovery from the pancytopenia, thus eliminating the need for diagnostic bone marrow aspiration.

It is our belief that plasmodium vivax should be listed as one of the causes of hemophagocytic syndrome. Diagnostic bone marrow aspiration should not be recommended in patients with known plasmodium vivax and pancytopenia, since these patients respond quickly to oral chloroquine. Repeated peripheral blood smears are very essential to reduce false negative results and subsequent misdiagnosis in this type of presentation. Malaria should be considered in the differential diagnosis of fever and pancytopenia in all travelers from endemic areas.

 
   References Top

1.Janka GE. Hemophagocytic syndromes. Blood Reviews 2007; 21; 245-53  Back to cited text no. 1
    
2.Retornaz F, Seux V, Arnoulet C, Durand JM, Sainty D, Soubeyrand J. Plasmodium falciparum malaria infection complicated by haemophagocytic syndrome in an old man. Acta Haematol 2000; 103:224-5.  Back to cited text no. 2
    
3.Fisman DN. Hemophagocytic syndromes and infection. Emerg Infect Dis 2000; 6:601-8.  Back to cited text no. 3
    
4.Yamakawa H, Kiyotaki M, Hattori Y, Obana M, Matsuoka Y, Irimajiri S. A case of Plasmodium vivax malaria complicated with pancytopenia due to hypoplasia of the bone marrow. Kansenshogaku zasshi 1989 ;63(9):1043-6  Back to cited text no. 4
    
5.Mohapatra MK, Padhiary KN, Mishra DP, Sethy G. Atypical manifestations of Plasmodium vivax malaria. Indian J Malariol 2002; 39(1-2):18-25.   Back to cited text no. 5
    
6.Aouba ME. Haemophagocytic syndrome associated with Plasmodium vivax infection. British Journal of Hematology 2000; 108; 832-3.  Back to cited text no. 6
    
7.Park TS, Oh SH, Chi JC, Kim HH, Chang CL, Son HC, Lee EY. Plasmodium vivax Malaria Complicated by Hemophagocytic Syndrome in an Immunocompetent Serviceman. American Journal of Hematology 2003; 74:127-30.   Back to cited text no. 7
    
8.Zvulunov A, Tamary H, Gal N, Pancytopenia resulting from hemophagocytosis in malaria. The Pediatric Infectious Disease Journal. 2002 ;21(11):1086-7.  Back to cited text no. 8
    



 
 
    Tables

  [Table 1], [Table 2]



 

Top
 
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
    Abstract
   Introduction
   Case Report
   Discussion
    References
    Article Tables

 Article Access Statistics
    Viewed2538    
    Printed93    
    Emailed0    
    PDF Downloaded298    
    Comments [Add]    

Recommend this journal

Advertise | Sitemap | What's New | Feedback | Disclaimer
Journal of Family and Community Medicine | Published by Wolters Kluwer - Medknow
Online since 05th September, 2010