eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease

Lymphadenitis

Author: Ulfat Shaikh, MD, MPH, Assistant Professor of Pediatrics, Department of Pediatrics, University of California Davis Medical Center
Coauthor(s): Dean A Blumberg MD, Associate Professor of Pediatrics, Section of Pediatric Infectious Disease, University of California Davis School of Medicine; Acting Chief, Section of Pediatric Infectious Disease, UC Davis Medical Center
Contributor Information and Disclosures

Updated: Apr 23, 2010

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Introduction

Background

Lymphadenitis is the inflammation and/or enlargement of a lymph node. Lymph node enlargement is common in children. Most cases represent a response to benign, local, or generalized infections (usually viral).1 Lymphadenitis may affect a single node or a localized group of nodes (regional adenopathy) and may be unilateral or bilateral. The onset and course of lymphadenitis may be acute, subacute, or chronic.2

Most children with lymphadenitis exhibit small palpable cervical, axillary, and inguinal nodes. Approximately 5% of these children have palpable suboccipital or postauricular nodes. Palpable supraclavicular, epitrochlear, and popliteal nodes are uncommon, as are mediastinal or abdominal nodes that are detected with radiographic studies.

Pathophysiology

Increased node size may be caused by the following:

  • Multiplication of cells within the node, including lymphocytes, plasma cells, monocytes, or histiocytes
  • Infiltration of cells from outside the node, such as malignant cells or neutrophils
  • Draining of a source of infection by lymph nodes

If the cause of adenopathy is not evident, consider congenital or neoplastic causes.

Frequency

United States

Lymph nodes are usually small and firm. They are palpable in the cervical, axillary, inguinal, and occipital regions of healthy infants and children. Multiple nodes, especially if present with splenomegaly, may be associated with human immunodeficiency virus (HIV) infection.

International

Tuberculous lymphadenitis can be seen in developing countries.

Mortality/Morbidity

Nodes may be large and may cause local pain and tenderness. Overlying skin may be erythematous. Neck stiffness and torticollis may occur because of cervical lymphadenopathy. Inflammation of retropharyngeal nodes (retropharyngeal abscess) may lead to dysphagia or dyspnea.

Mediastinal lymphadenitis may cause cough, dyspnea, stridor, dysphagia, pleural effusion, and venous congestion in the upper body. Intra-abdominal (mesenteric and retroperitoneal) adenopathy may manifest as abdominal pain. Iliac lymph node involvement may cause abdominal pain and limping.

Clinical

History

The history in patients with lymphadenitis may include the following:

  • Upper respiratory symptoms, sore throat, earache, coryza, conjunctivitis, and impetigo
  • Fever, irritability, and anorexia
  • Contact with animals, especially kittens

Dental care

Submaxillary adenopathy may develop secondary to stomatitis, dental caries, or a dental abscess.

Risk factors for tuberculosis3

Generalized lymphadenopathy in a child with tuberculosis may indicate a hematogenous spread of tubercle bacilli.

Localized involvement is most common in the mediastinal, mesenteric, or anterior cervical nodes.

Acute or chronic onset

Usually, bilateral acute cervical adenitis is caused by either viral pharyngitis or infectious mononucleosis.

Chronic localized adenopathy can be attributed to a persistent regional infection.

Skin and scalp conditions

Occipital and postauricular adenopathy may accompany scalp infections, seborrheic dermatitis, or scalp pediculosis. Epitrochlear and axillary lymphadenopathy may result from infections on the arms. Inguinal and femoral adenopathy may be due to infections on the lower extremities.

Periodicity

Periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome usually results in adenopathy associated with the other findings every 3-6 weeks.

History of travel

When adenopathy is caused by Yersinia pestis (bubonic plague), the patient may have visited a rural area in the western United States one week prior to the onset of illness.

Medication use

The following medications may have been used:

  • Hydantoin
  • Mesantoin

Age

Atypical mycobacteria typically cause adenopathy in toddlers.

Physical

Physical findings may include the following:

Location

Tularemia may be accompanied by regional adenopathy, most commonly cervical.

Yersinia enterocolitica infection may cause cervical or abdominal adenopathy.

Salmonella infections may accompany generalized lymphadenopathy.

Rubella and parvovirus infection is characterized by enlarged and tender posterior auricular, posterior cervical, and occipital lymph nodes.

Atypical (environmental) mycobacteria may cause submandibular or submental adenopathy.

Mediastinal or infectious hilar adenopathy may occur in patients with tuberculosis, chronic sinusitis, histoplasmosis, tularemia, infectious mononucleosis, candidiasis, coccidioidomycosis, and bronchiectasis.

Size

Lymph nodes that are noted to increase rapidly in size may indicate potential malignancy.

Shape

Confluent lymph nodes may be indicators of malignancy.

Consistency

Descriptors may include soft, fluctuant, firm, rubbery, or hard.

In early stages, nodes in tuberculosis are well-demarcated, mobile, nontender, and firm. If the infection remains untreated, the nodes soften, become fluctuant, and adhere to the skin, which may be erythematous.

In Hodgkin disease, nodes are initially soft. They later become firm and rubbery.

Fixation of lymph nodes to the skin and soft tissue may indicate malignancy.

Tenderness

Lymph nodes of infectious etiology are usually tender.

Bubonic plague, caused by Y pestis, may cause extremely tender lymph node enlargement and erythema of overlying skin in the inguinal, femoral, axillary, or cervical area.

Hodgkin lymphoma may initially present as painless lymph node enlargement, especially of the cervical and supraclavicular region.

Overlying skin

The overlying skin may be erythematous in infectious etiologies.

Draining sinuses may develop in patients with tuberculous adenopathy.

Infants with atopic eczema may have generalized lymphadenopathy.

Systemic signs

Group B streptococcal cellulitis and adenitis, which may occur in infants younger than 2 months, are characterized by sudden onset of fever, anorexia, irritability, and submandibular swelling. Usually, a blood culture test demonstrates positive results.

Hepatosplenomegaly is common in patients with infectious mononucleosis.

Conjunctivitis

Preauricular adenopathy (Parinaud oculoglandular syndrome) secondary to uniocular granulomatous conjunctivitis may be caused by catscratch disease, chlamydial conjunctivitis, listeriosis, tularemia, or tuberculosis.

Adenovirus type 3 causes pharyngeal conjunctival fever. Symptoms associated with adenovirus type 3 include follicular conjunctivitis with enlarged preauricular and/or posterior cervical nodes. Adenovirus type 8 causes epidemic keratoconjunctivitis, which causes preauricular adenopathy.

PFAPA syndrome

Aphthous stomatitis and pharyngitis are associated with PFAPA syndrome.

Number

A single node or multiple nodes may be involved.

Catscratch disease

In catscratch disease, usually only a single node is involved.

Causes

Causes of lymphadenitis include the following:

Infections

Acute, one-sided, pyogenic adenitis is most common. The involved node may be firm and tender, with erythema of the overlying skin. Etiologic agents include group A beta-hemolytic streptococci, staphylococcal organisms (especially Staphylococcus aureus),4 and viruses.

Tularemia may be accompanied by regional adenopathy, most commonly cervical, with local tenderness, pain, and fever. Generalized lymphadenopathy may also develop.5

In a child with tuberculosis, generalized lymphadenopathy may indicate hematogenous spread of tubercle bacilli. Localized involvement is most common in the mediastinal, mesenteric, or anterior cervical nodes. Initially, the nodes are discrete, firm, mobile, and tender. If the patient remains untreated, the nodes soften, become fluctuant and matted, and adhere to overlying skin, which may become erythematous. Bilateral involvement is characteristic of this condition. Pulmonary disease is common.

Atypical mycobacteria can manifest cervical or submandibular involvement identical to that of tuberculosis, except the involvement is usually unilateral.6

Group B streptococcal cellulitis and adenitis may occur in infants younger than 2 months.

Brucellosis may accompany chronic or intermittent lymphadenopathy.

Y enterocolitica may be associated with cervical lymphadenitis.

Salmonella infection can correspond to generalized adenopathy.

Bubonic plague is caused by Y pestis.

In patients with catscratch disease, the site of the scratch determines if axillary, epitrochlear, supraclavicular, femoral, inguinal, or submaxillary lymph nodes are involved. The nodes are nontender, discrete, mobile, and moderately or greatly enlarged. Occasionally, tenderness, redness, warmth, and suppuration may occur. Bartonella henselae is the organism that causes catscratch disease.

Patients with infectious mononucleosis typically present with discrete, firm, nontender lymph nodes. Usually, anterior cervical nodes are involved. Generalized lymphadenopathy may occur, and hepatosplenomegaly is common.

Cytomegalovirus or toxoplasmosis may cause a mononucleosislike syndrome with generalized adenopathy, fever, atypical lymphocytes, and hepatosplenomegaly.

Gianotti-Crosti syndrome accompanies generalized lymphadenopathy, hepatomegaly, splenomegaly, nonicteric hepatitis, and crops of papular lesions that persist for 2-8 weeks.

Immunologic or connective tissue disorders

Juvenile rheumatoid arthritis should be considered in unexplained fever and persistent lymphadenopathy in a child.

Serum sickness can correspond with generalized tender lymphadenopathy.

Chronic graft versus host disease may occur.

Primary disease of lymphoid or reticuloendothelial tissue

These include the following:

  • Acute leukemia
  • Lymphosarcoma
  • Reticulum cell sarcoma
  • Hodgkin disease
  • Non-Hodgkin lymphoma
  • Malignant histocytosis or histocytic lymphoma
  • Nonendemic Burkitt tumor
  • Nasopharyngeal rhabdomyosarcoma
  • Neuroblastoma7
  • Thyroid carcinoma, chronic lymphocytic thyroiditis
  • Histiocytosis X
  • Kikuchi disease8
  • Benign sinus histiocytosis
  • Angioimmunoblastic or immunoblastic lymphadenopathy
  • Chronic pseudolymphomatous lymphadenopathy (chronic benign lymphadenopathy)

Immunodeficiency syndromes and phagocytic dysfunction

These include the following:

Metabolic and storage diseases

These include the following:

Hematopoietic diseases

These include the following:

Other disorders

Kawasaki disease usually presents with cervical adenopathy that is unilateral and with nodes that are firm, nontender, and greater than 1.5 cm in diameter.9 Overlying skin may be erythematous but not warm.10

PFAPA syndrome usually occurs in young children (onset almost always before age 5 y) and is remarkable because of its regular periodicity. All findings may not occur in each patient. Children are otherwise healthy between episodes and display normal growth and development. During the acute episodes, elevation of inflammatory markers (eg, WBC count, erythrocyte sedimentation rate) is often present. A recent study determined that the Gaslini diagnostic score is a useful tool in differentiating PFAPA syndrome from monogenic periodic fevers.11

Drug use can affect lymph nodes. Mesantoin use may cause enlargement of lymph nodes (most commonly in the cervical region), fever, eosinophilia, rash, and hepatosplenomegaly. Hydantoin use also may produce lymphadenopathy as an adverse effect.

Almost all patients with sarcoidosis demonstrate either generalized or hilar lymphadenopathy. When enlarged, bilateral cervical nodes are firm, rubbery, and discrete, with little tendency to coalesce. Other symptoms include fatigue, cough, fever, dyspnea, and weight loss. Hyperglobulinemia and eosinophilia are common laboratory findings.

Castleman disease or benign giant lymph node hyperplasia may cause lymphadenopathy in the mediastinum, abdomen, neck, or axilla. Some patients experience fever, anemia, weight loss, and hyperglobulinemia.

More on Lymphadenitis

Overview: Lymphadenitis
Differential Diagnoses & Workup: Lymphadenitis
Treatment & Medication: Lymphadenitis
Follow-up: Lymphadenitis
Multimedia: Lymphadenitis
References

References

  1. Leung AK, Davies HD. Cervical lymphadenitis: etiology, diagnosis, and management. Curr Infect Dis Rep. May 2009;11(3):183-9. [Medline].

  2. Friedmann AM. Evaluation and management of lymphadenopathy in children. Pediatr Rev. Feb 2008;29(2):53-60. [Medline].

  3. Fraser L, Moore P, Kubba H. Atypical mycobacterial infection of the head and neck in children: a 5-year retrospective review. Otolaryngol Head Neck Surg. Mar 2008;138(3):311-4. [Medline].

  4. Guss J, Kazahaya K. Antibiotic-resistant Staphylococcus aureus in community-acquired pediatric neck abscesses. Int J Pediatr Otorhinolaryngol. Jun 2007;71(6):943-8. [Medline].

  5. Guffey MB, Dalzell A, Kelly DR, Cassady KA. Ulceroglandular tularemia in a nonendemic area. South Med J. Mar 2007;100(3):304-8. [Medline].

  6. Carvalho AC, Codecasa L, Pinsi G, et al. Differential Diagnosis of Cervical Mycobacterial Lymphadenitis in Children. Pediatr Infect Dis J. Feb 12 2010;[Medline].

  7. Pepper S, Islam HK, Jayabose S, et al. Neuroblastoma masquerading as cervical lymphadenitis. J Pediatr Hematol Oncol. Apr 2007;29(4):260-1. [Medline].

  8. Chuang CH, Yan DC, Chiu CH, et al. Clinical and laboratory manifestations of Kikuchi's disease in children and differences between patients with and without prolonged fever. Pediatr Infect Dis J. Jun 2005;24(6):551-4. [Medline].

  9. [Guideline] Newburger JW, Takahashi M, Gerber MA, et al. Diagnosis, treatment, and long-term management of Kawasaki disease: a statement for health professionals from the Committee on Rheumatic Fever, Endocarditis and Kawasaki Disease, Council on Cardiovascular Disease in the Young, American Heart Association. Circulation. Oct 26 2004;110(17):2747-71. [Medline].

  10. Rigante D, La Torraca I, Rossodivita A, et al. Unilateral cervical mass as a main clue raising the diagnostic suspicion of Kawasaki syndrome. Rheumatol Int. Nov 2007;28(1):73-6. [Medline].

  11. Gattorno M, Caorsi R, Meini A, et al. Differentiating PFAPA syndrome from monogenic periodic fevers. Pediatrics. Oct 2009;124(4):e721-8. [Medline].

  12. Simanovsky N, Hiller N. Importance of sonographic detection of enlarged abdominal lymph nodes in children. J Ultrasound Med. May 2007;26(5):581-4. [Medline].

  13. Balaji J, Sundaram SS, Rathinam SN, Rajeswari PA, Kumari ML. Fine needle aspiration cytology in childhood TB lymphadenitis. Indian J Pediatr. Dec 2009;76(12):1241-6. [Medline].

  14. Ahuja A, Ying M, Yuen YH, Metreweli C. Power Doppler sonography of cervical lymphadenopathy. Clin Radiol. Dec 2001;56(12):965-9. [Medline].

  15. Chao SS, Loh KS, Tan KK, Chong SM. Tuberculous and nontuberculous cervical lymphadenitis: A clinical review. Otolaryngol Head Neck Surg. Feb 2002;126(2):176-9. [Medline].

  16. Elden LM, Grundfast KM, Vezina G. Accuracy and usefulness of radiographic assessment of cervical neck infections in children. J Otolaryngol. Apr 2001;30(2):82-9. [Medline].

  17. Eriksson M, Bennet R, Danielsson N. Non-tuberculous mycobacterial lymphadenitis in healthy children: another "lifestyle disease"?. Acta Paediatr. Nov 2001;90(11):1340-2. [Medline].

  18. Green M. Lymphadenopathy. In: Pediatric Diagnosis. 5th ed. WB Saunders Co; 1992:393-7.

  19. Hazra R, Robson CD, Perez-Atayde AR, Husson RN. Lymphadenitis due to nontuberculous mycobacteria in children: presentation and response to therapy. Clin Infect Dis. Jan 1999;28(1):123-9. [Medline].

  20. Koybasi S, Saydam L, Gungen Y. Histiocytic necrotizing lymphadenitis of the neck. Am J Otolaryngol. Sep-Oct 2003;24(5):344-7. [Medline].

  21. Loeffler AM. Treatment options for nontuberculous mycobacterial adenitis in children. Pediatr Infect Dis J. Oct 2004;23(10):957-8. [Medline].

  22. Peters TR, Edwards KM. Cervical lymphadenopathy and adenitis. Pediatr Rev. Dec 2000;21(12):399-405. [Medline].

  23. Thomas KT, Edwards KM. Periodic fever syndrome. Pediatr Infect Dis J. Jan 1999;18(1):68-9. [Medline].

Further Reading

Keywords

lymphadenitis, adenopathy, lymphadenopathy, lymph node enlargement, lymph node inflammation, lymph node infection, periodic fever, PFAPA syndrome, Kawasaki disease, Castleman disease, benign giant lymph node hyperplasia

Contributor Information and Disclosures

Author

Ulfat Shaikh, MD, MPH, Assistant Professor of Pediatrics, Department of Pediatrics, University of California Davis Medical Center
Ulfat Shaikh, MD, MPH is a member of the following medical societies: American Academy of Pediatrics and American Public Health Association
Disclosure: Nothing to disclose.

Coauthor(s)

Dean A Blumberg MD, Associate Professor of Pediatrics, Section of Pediatric Infectious Disease, University of California Davis School of Medicine; Acting Chief, Section of Pediatric Infectious Disease, UC Davis Medical Center
Dean A Blumberg MD is a member of the following medical societies: American Academy of Pediatrics, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, California Medical Association, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Sierra Sacramento Valley Medical Society
Disclosure: Novartis Grant/research funds clinical research investigator; Merck speaking fees paid to university, not self Speaking and teaching; sanofi pasteur speaking fees paid to university, not self Speaking and teaching

Medical Editor

Gary J Noel, MD, Department of Pediatrics, Clinical Associate Professor, Weill Medical College of Cornell University
Gary J Noel, MD is a member of the following medical societies: Pediatric Infectious Diseases Society
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Larry I Lutwick, MD, Professor of Medicine, State University of New York, Downstate Medical School; Director, Infectious Diseases, Veterans Affairs New York Harbor Health Care System, Brooklyn Campus
Larry I Lutwick, MD is a member of the following medical societies: American College of Physicians and Infectious Diseases Society of America
Disclosure: Nothing to disclose.

CME Editor

Robert W Tolan Jr, MD, Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine
Robert W Tolan Jr, MD is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, Phi Beta Kappa, and Physicians for Social Responsibility
Disclosure: GlaxoSmithKline Honoraria Speaking and teaching; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; sanofi pasteur Honoraria Speaking and teaching; Baxter Healthcare Honoraria Speaking and teaching; Novartis Honoraria Speaking and teaching

Chief Editor

Russell W Steele, MD, Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine
Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association
Disclosure: None None None

 
 
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