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Lymphadenopathy in African Children  247

            The node sampled should be a representative node, preferably from   Up to 18% of HIV-affected patients in Africa have lymphadenopathy
          a deep site. The node should be divided into specimens for histology   on presentation. A generalised lymphadenopathy (particularly cervical
          and specimens for tissue culture (and TB culture). The specimen for   and axillary nodes) has been reported as the most common presentation
          histology should be further divided into a formalin fixed section and a   of  children  with  symptomatic  HIV  in  Zimbabwe,  but  concomitant
          section sent fresh for imprinting. Figure 37.9 outlines the handling of   tuberculosis  needs  to  be  excluded.  The  histological  picture  of  HIV-
          biopsy specimens.                                      affected lymphadenopathy is usually nonspecific with the immunologic
            The surgical technique for lymph node excision is shown in Figure 37.10.  reaction to HIV being the most prominent feature. The picture is further
          Immunocompromised Patient                              complicated by the clinical and multiple HIV virus subtypes in sub-
          Lymphadenopathy may be a much more serious problem in the immu-  Saharan Africa and Nigeria.
          nocompromised patient.


                                                    Key Summary Points

              1.  Lymphadenopathy is an extremely common clinical finding in   9.  A special situation exists in lymphadenopathy related to the
                the children of Africa as well as the rest of the world.    Danish strain of bacille Calmette-Guérin, (BCG) particularly in
                                                                    immunocompromised children.
              2.  It is most prevalent in the first decades of life and the majority
                of children between the ages of 2 and 12 will have an enlarged   10. Up to 18% of HIV affected patients in Africa have
                lymph node at one stage or another.                 lymphadenopathy on presentation.
              3.  A significant lymph node is >2cm.              11. Malignancy in enlarged lymph nodes occurs in 12% and 2/3
                                                                    are lymphomas.
              4.  Lymphadenopathy may be the first (and sometimes only)
                indication of underlying disease.                12. Fine needle Aspiration biopsy (FNAB) is a useful triage for the
                                                                    rapid and definitive diagnosis of tuberculosis but may miss
              5.  Active management is justified of paediatric patients with   malignancy.
                persisting lymphadenopathy.
                                                                 13. Early tissue sampling indicated with generalized symptoms
              6.  Atypical anatomic regions, persistence despite appropriate   of unexplained fever and weight loss.and lymphadenopathy
                treatment, absence of previous pyogenic infection,   (especially mediastinal and abdominal lymph nodes.
                geographical prevalence, history of cat scratch, a positive TB
                history, are all important in assessment.        14. Where malignancy is suspected biopsy of an entire
                                                                    representative lymph node is required and submitted for
              7.  The aetiology is mostly infective. This may be acute bacterial,   appropriate culture and histology.
                viral or chronic inflammation due to many different infective
                agents.
              8.  Granulomas suggest chronic infective causes such as
                mycobacteria (e.g., M. tuberculosis and other mycobacteria]
                organisms.




                                                         References
             1.   Moore SW, Schneider JW, Schaaf HS. Diagnostic aspects of   4.   Mutalima N, Molyneux E, Jaffe H, Kamiza S, Borgstein E,
                 cervical lymphadenopathy in children in the developing world: a   Mkandawire N, et al. Associations between Burkitt lymphoma
                 study of 1,877 surgical specimens. Pediatr Surg Int 2003; 19:240–  among children in Malawi and infection with HIV, EBV and malaria:
                 244.                                               results from a case-control study. PLoS ONE 2008; 3(6):e2505.
             2.   Zeharia A, Eidlitz-Markus T, Haimi-Cohen Y, Samra Z, Kaufman   5.   Wright CA, van der BM, Geiger D, Noordzij JG, Burgess SM,
                 L, Amir J. Management of nontuberculous mycobacteria-induced   Marais BJ. Diagnosing mycobacterial lymphadenitis in children
                 cervical lymphadenitis with observation alone. Pediatr Infect Dis J   using fine needle aspiration biopsy: cytomorphology, ZN staining
                 2008; 27:920–922.                                  and autofluorescence—making more of less. Diagn Cytopathol
                                                                    2008; 36:245–251.
             3.   Foucar E, Rosai J, Dorfman R. Sinus histiocytosis with massive
                 lymphadenopathy (Rosai-Dorfman disease): review of the entity.
                 Semin Diagn Pathol 1990; 7:19–73.
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