Lymphadenopathy
Leslie S. Kersun
INTRODUCTION
Healthy children frequently have palpable lymph nodes, most commonly in the cervical, axillary, and inguinal areas. There is a broad differential diagnosis for lymphadenopathy in children. This enlargement can be suggestive of underlying disease, so it is important to have an organized and thoughtful approach to the evaluation of a child with lymphadenopathy. Lymph nodes can enlarge secondary to proliferation of normal lymphocytes (infection or lymphoproliferative process) or from migration and infiltration of nodal tissue by extrinsic inflammatory or metastatic malignant cells.
There are a number of factors to consider that will help narrow the differential diagnosis. These include:
Patient age: Lymph nodes in the cervical, axillary, and inguinal region are frequently palpated in early childhood.
Size: Anterior cervical and axillary nodes >1 cm or inguinal nodes >1.5 cm require further investigation. Enlarged supraclavicular nodes can reflect mediastinal or abdominal pathology and should always be considered pathologic.
Location: Important to understand the patterns of drainage in order to carefully look for infection or inflammation. Examples include:
Anterior cervical nodes drain the mouth/pharynx: Upper respiratory infection
Occipital and posterior cervical nodes drain the scalp: Tinea capitis
Preauricular: Conjunctivitis, external ear infections
Axillary: Cat-scratch disease
Submental: dental infections, gingivostomatitis
Quality (tender, warm, firm, erythematous): Requires further evaluation for infectious process.
Area: localized versus generalized
Length of time: Differential diagnosis varies for acute nodal enlargement (usually <3 to 4 weeks) versus chronic enlargement (>4 to 6 weeks).
Presence of systemic symptoms: Weight loss, rash, fever, night sweats
DIFFERENTIAL DIAGNOSIS LIST
Lymphadenopathy in Children
Infectious Causes Bacterial Infection
Localized:
Staphylococcus aureus
Group A Streptococcus (pharyngitis)
Anaerobes
Tularemia
Diphtheria
Chancroid
Atypical mycobacterium
Cat-scratch disease (Bartonella henselae)
Generalized:
Lymphogranuloma venereum
Leptospirosis
Bacteremia
Scarlet fever
Syphilis
Tuberculosis (TB)
Subacute bacterial endocarditis
Brucellosis
Leptospirosis
Typhoid fever
Plague
Lyme disease
Tularemia
Viral Infection
Epstein-Barr virus (EBV)
HIV
Varicella
Cytomegalovirus (CMV)
Rubeola
Rubella
Infectious hepatitis
Influenza
Upper respiratory viral infection such as parainfluenza, rhinovirus, respiratory syncytial virus
Fungal Infection
Histoplasmosis
Coccidioidomycosis
Parasitic Infection
Toxoplasmosis
Malaria
Neoplastic
Primary Lymphoid Neoplasm
Lymphoma
Leukemia
Metastatic Neoplasm
Neuroblastoma
Rhabdomyosarcoma
Thyroid carcinoma
Nasopharyngeal carcinoma
Metabolic
Gaucher disease
Niemann-Pick disease
Immunologic
Systemic lupus erythematosus
Juvenile rheumatoid arthritis
Vasculitis syndromes
Serum sickness
Autoimmune hemolytic anemia
Chronic granulomatous disease
Autoimmune lymphoproliferative syndrome
Medications
Dilantin
Isoniazid
Immunizations
Endocrine
Hyperthyroidism
Histiocytoses
Miscellaneous
Kawasaki syndrome
Skin disorders
Atopic dermatitis
Sarcoidosis
Castleman disease (benign giant lymph node hyperplasia)
Kikuchi-Fujimoto disease
DIFFERENTIAL DIAGNOSIS DISCUSSION
Lymphadenitis
Etiology
Acute infective lymphadenitis is a problem frequently encountered in the pediatric population. It represents a primary infection of the lymph node. The causative organism frequently gains entry into the body through the pharynx, nares, dentition, or a break in the skin. The etiology is most often bacterial, with S. aureus being the most frequently isolated organism. Other pathogens that may be found include group A streptococci, Mycobacterium tuberculosis, atypical mycobacteria, gram-negative bacilli (such as B. henselae), Haemophilus influenzae, anaerobic bacteria, Francisella tularensis, and Yersinia pestis.
Clinical Features
Physical examination usually reveals a unilateral, tender, warm, often fluctuant lymph node with erythema of the overlying skin. Fever and elevated white blood cell count occur occasionally, most often in the younger child.
Evaluation and Treatment
Aspiration often reveals the cause and may provide symptomatic relief if the lymph node is large or in an awkward position. In uncomplicated cases, treatment with an oral antibiotic is frequently all that is needed. Recent increases in antibiotic resistance such as methicillin-resistant S. aureus may impact the choice of antibiotics. Infants, children who appear clinically ill or have an underlying immunodeficiency, those who do not improve or progress on oral antibiotics and those who develop associated cellulitis should be admitted to the hospital for intravenous antibiotics and further evaluation.
Reactive Lymphadenopathy
Etiology
Reactive hyperplasia of lymph nodes represents a response to antigenic stimuli (foreign material, cellular debris, or infectious organisms and their toxic products).
Clinical Features
The resulting lymphadenopathy can be acute or chronic. The cervical, axillary, and inguinal nodes are most commonly involved and can sometimes grow to be quite large. The nodes clinically enlarge secondary to infiltration with histiocytes or plasma cells. Acute cellular infiltration and edema causes distention of the capsule, producing tenderness when the lymph node is palpated.
Evaluation
In the acute setting: Careful history and physical examination, with attention to symptoms of upper respiratory infections (influenza or adenovirus are commonly associated with cervical lymphadenopathy), symptoms of EBV or CMV, local infections of the ear, nose, teeth, or skin, or Kawasaki disease.
In chronic situations: Chronic lymph node hyperplasia can pose a diagnostic dilemma (see section on “Evaluation of Lymphadenopathy”). Lymph node biopsy may be helpful and usually recommended when the lymph node has been enlarged for more than 4 to 6 weeks without a clear cause. In children who undergo lymph node biopsies, the majority (˜75%) are reactive or benign. Lymph nodes infiltrated with malignancy are more likely to be supraclavicular in location, chronic (present for >4 weeks), >3 cm, and in patients with some abnormality on laboratory testing or imaging.Stay updated, free articles. Join our Telegram channel
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