Page 9 - 64 head&neck36-40_opt
P. 9

242  Lymphadenopathy in African Children

           Cervical lymphadenopathy has been reported to occur in 4–9% of   antituberculous therapy, surgical excision has become the treatment of
        children  with  pulmonary  tuberculosis,  with  57%  occurring  between   choice  for  nontuberculous  mycobacterial  lymphadenopathy.  Surgical
        the ages of 1 and 3 years. Clinical suspicion of cervical TB is high in   management  encompasses  total  excision  or  curettage  of  the  affected
        children with a previous history of TB or close contact with a TB patient   lymph node(s) and remains the treatment of choice due to the high cure
        from an endemic region. The significance increases in the presence of a   rate with a single procedure. For lesions in proximity to the facial nerve
        markedly positive tuberculin skin test (i.e., Mantoux test). The finding   or with extensive skin necrosis, curettage can be performed as an alter-
        of  nontender,  painless,  unilateral  cervical  lymph  nodes  on  physical   native to total excision as the initial procedure. This is usually part of
        examination further strengthens this suspicion. Objective diagnosis is   a staged process followed by subsequent excision and wound closure.
        then fairly difficult and relies on cervical lymph node sampling.  Immunocompetent  patients  with  nontuberculous  cervical
           Particular difficulties exist in making a clinical diagnosis in children   lymphadenitis do, however, appear to show some response to medical
        with HIV disease, who may have atypical presentations. When clinically   therapy  alone.  A  recent  study   of  92  immunocompetent  children
                                                                                       2
        indicated,  screening  for  pulmonary  and  laryngeal  disease  depends   with nontuberculous mycobacterial lymphadenopathy (90% M. avium
        heavily on lymph node sampling. Fine needle aspiration (FNA) with   complex  or  M.  hemophilum)  showed  a  natural  history  of  violaceous
        culture  or  polymerase  chain  reaction  (PCR)–based  identification  are   skin changes with discharge of pus for 3–8 weeks. The infection then
        rapidly overtaking the more conventional methods of diagnosis, with   seemed to settle, with 71% achieving total resolution within 6 months
        the  more  traditional  method  of  excisional  biopsy  being  reserved  for   and resolution of the remaining 29% within 9–12 months. This raises
        selected cases.                                        the  question  of  a  possible  conservative  approach  to  nontuberculous
        Nontuberculous Mycobacterial Infections                mycobacterial infestations of the cervicocranial region.
                                                                 Cervical lymphadenopathy caused by nontuberculous mycobacteria
        BCG lymphadenitis                                      can  thus  be  managed  by  a  variety  of  therapeutic  options  in
        A  special  situation  exists  in  lymphadenopathy  related  to  the  Danish   immunoincompetent  children,  with  infection  resolution  being  the
        strain of bacille Calmette-Guérin (BCG; Figure 37.3), which is estimat-  eventual  outcome  regardless  of  management  option  selected.  The
        ed to occur at the rate of 36 per 1,000 vaccinations. This may be partly   best management option in this group appears to be an individualised
        strain specific, and the association of the current Danish-strain BCG   approach  with  excisional  biopsy  as  the  recommended  option;  its
        and  regional  lymphadenitis  has  been  recognised  especially  in  HIV-  feasibility is determined by the length of history, the danger of facial
        positive children. Similarly, disseminated BCG disease occurs almost   nerve injury (due to position), and the presence of hypertrophic scarring.
        exclusively  in  immunocompromised  children  and  has  an  extremely   In  immunocompromised  (e.g.,  HIV-affected)  children,  the
        high mortality. In HIV-positive children with suspected BCG-regional   management  option  may  change  depending  on  the  CD4  count.  The
        axillary lymphadenitis, the diagnosis should be confirmed by means of   potential  for  systemic  disease  in  these  patients  remains  (see  the
        FNA, pus swab, or gastric washout. The investigative protocol in these   preceding section on bacille Calmette-Guérin lymphadenitis).
        patients  should  include  a  chest  radiograph  to  exclude  disseminated   Other Causes of Chronic Granulomas in Lymph Nodes
        mycobacterial disease. If a positive BCG mycobacterium is cultured
        from the lymph nodes, initial treatment should be by means of tubercu-  Rosai-Dorfman disease
        lostatics, and surgery should be avoided and reserved for complicated   Rosai-Dorfman disease, or sinus histiocytosis with massive lymphade-
        patients and cases where diagnostic doubt exists.      nopathy (SHML), is an uncommon but well-defined cause of chronic
           In BCG adenitis, if the lymph nodes are <3 cm in size, the diagnostic   lymphadenopathy in childhood. It is a histiocytic proliferative disease.
        FNA  should  be  followed  by  a  “wait  and  see”  policy,  which  avoids   Patients may present with a low-grade fever and cervical lymphade-
        the  use  of  ineffective  tuberculostatics,  with  the  inherent  problem  of   nopathy.  It  is  a  benign  self-limiting  disorder.  Histological  features
        acquired  drug  resistance,  as  well  as  affording  a  lower  incidence  of   include  numerous  large  histiocytes  with  prominent  emperipolesis  (a
        surgically related complications. In nodes >3 cm in size with a negative   halo  observed  around  the  cell),  fine  vacuoles  in  the  cytoplasm,  and
        FNA culture, other concerns of underlying disease need to be taken into   lymphocytes and plasma cells in the background.
        account in evaluating surgical intervention. This is especially so if the   Diagnosis  has  successfully  been  made  with  a  FNA  biopsy  in  a
        patient is not responding to conventional therapy.     number  of  reports  demonstrating  the  characteristic  SHML  features,
        Mycobacteria other than tuberculosis                   namely, large histiocytes with abundant pale, eosinophilic cytoplasm
        Mycobacteria other than tuberculosis can be a cause of chronic localised   containing  well-preserved  lymphocytes  and  occasional  plasma  cells
        cervicofacial  lymphadenitis.  Due  to  MOTT’s  perceived  resistance  to   and granulocytes. Additional immunostaining may demonstrate typical
                                                               positive S-100 protein and alpha-1-antichymotrypsin staining, but no
                                                               reaction when stained for lysozyme.
                                                               Cat scratch disease
                                                               Cat scratch disease is caused by infection by the Bartonella henselae
                                                               organism.  Cat  scratch  disease  occurs  in  many  countries  (including
                                                               some developing ones), but may be difficult to diagnose in children. It
                                                               is a self-limiting zoonotic condition that may occur at any age, but it
                                                               is most common among children and adolescents. It usually involves
                                                               enlargement of only a single node regionally, which is usually the cer-
                                                               vical or axillary and very rarely inguinal lymph nodes. It is diagnosed
                                                               on careful history taking and specific serological test and histopatho-
                                                               logical examination.
                                                               Castleman disease
                                                               Castleman disease (angiofollicular lymph node hyperplasia) has been
                                                               reported in Africa both in the cervicofacial area and intraabdominally.
                                                               Although presentation as an asymptomatic neck mass is not uncom-
        Figure 37.3: BCG ulcer (small arrow) and axillary lymphadenopathy (large   mon,  it  most  frequently  presents  with  mediastinal  lymphadenopathy.
        arrow) in a neonate.
   4   5   6   7   8   9   10   11   12   13   14