ConditionHistory/risk factorsPhysical findingsDiagnosisManagement
Acute
Acute sialadenitisOlder, debilitated persons with dehydration or recent dental proceduresRapid or gradual onset of pain and swelling; local edema, erythema, tenderness, or fluctuance consistent with an abscessContrast-enhanced CTSialagogues, gentle massage; abscess, express by compressing the gland
HematomaTraumaSoft, possible overlying ecchymosisUltrasonography or contrast-enhanced CTMonitor if small; surgical drainage if large or expanding
Pseudoaneurysm or arteriovenous fistulaTrauma with shearing forcesLateral; soft, pulsatile mass with a thrill or bruitCT with or without CT angiographySurgical evaluation for ligation
Reactive lymphadenopathy
Bartonella henselae infectionKitten or flea exposureIsolated, mobile, fluctuant, tender, warm, erythematous, > 2 cm near site of inoculationBartonella antibody titersAzithromycin (Zithromax)
CytomegalovirusURI symptomsRubbery, mobile, cervical, and generalized; > 2 cmCytomegalovirus titerBiopsy if no resolution after 8 weeks
Epstein-Barr virus infectionURI symptomsRubbery, mobile, cervical, and generalized; > 2 cmMonospot, Epstein-Barr virus titerBiopsy if no resolution after 8 weeks
HIV infectionBlood/sexual contactRubbery, mobile, cervical, and generalizedHIV enzyme-linked immunoassayHighly active antiretroviral therapy
Mycobacterium tuberculosis (extrapulmonary)Travel to or immigration from an endemic area, homelessness, immunocompromiseDiffuse, bilateral lymph nodes (multiple, fixed, firm, nontender)Purified protein derivative test to rule out atypical mycobacteria infection; acid-fast bacilli cultureAntibiotics: rifampin and isoniazid; add pyrazinamide and ethambutol or streptomycin in endemic areas; refer to a head and neck surgeon if persistent after initial diagnosis and treatment
Staphylococcal or streptococcal infectionSkin infectionsMobile, fluctuant, tender, warm, erythematousClinicalAntibiotics
ToxoplasmosisCat feces exposureRubbery, mobile, cervical, and generalizedToxoplasmosis antibody titerSupportive care or treat with pyrimethamine and sulfadiazine
Viral URIURI symptomsMobile, rubbery, bilateral; subsides in 3 to 6 weeksClinicalBiopsy if no resolution 3 to 6 weeks after symptom resolution
Subacute (weeks to months)
Cancer
Hodgkin lymphoma15 to 34 years of age and > 55 years, constitutional symptoms, later splenomegalyPainless, rapidly growing lymph node; rubbery, soft, mobileContrast-enhanced CT of the neck, chest, abdomen, pelvis; biopsyRefer to oncology
Human papillomavirus–related squamous cell carcinoma35- to 55-year-old white men with a history of smoking, heavy alcohol use, and multiple sex partners (especially involving orogenital contact)Rapidly enlarging, lateral, cystic lymph nodes; persistent cervical nodal hypertrophy; palatine or lingual tonsillar asymmetry; dysphagia; voice changes; pharyngeal bleedingNasal endoscopy, laryngoscopy, bronchoscopy with biopsies2-week trial of antibiotics; refer for biopsy if no resolution
Metastatic cancerHistory of melanoma or lung, breast, colon, genitourinary cancerMatted, firm, fixed lymph nodesContrast-enhanced CT of the neck, thorax, abdomen, pelvisRefer to oncology
Non-Hodgkin lymphomaOlder personsPainless, rapidly growing lymph node; rubbery, soft, mobile; may involve the tonsillar ring in the pharynxContrast-enhanced CT of the neck, chest, abdomen, pelvis; biopsyRefer to oncology
Parotid tumorsAsymptomaticSlow-growing, unilateral, mobile, asymptomatic; cranial nerve (often VII [facial]) involved if malignantContrast-enhanced CT and/or FNABRefer to ENT for excisional biopsy
Upper aerodigestive tract squamous cell carcinomaMale sex; use of tobacco, alcohol, betel nutNonhealing ulcers, dysarthria, dysphagia, odynophagia, loose or misaligned teeth, globus, hoarseness, hemoptysis, oropharyngeal paresthesiasNasal endoscopy, laryngoscopy, bronchoscopy with biopsies2-week trial of antibiotics; refer for biopsy if no resolution
Chronic sialadenitisMild to severe pain, often after mealsFirm glandCTSialagogues, gentle massage, refer to ENT
Idiopathic diseases
Castleman disease (angiofollicular lymphoproliferative disease)Constitutional symptomsSolitary lymph nodeContrast-enhanced CT (shows no enhancement, unlike lymphoma); FNABRefer to hematology
Kikuchi disease (histiocytic necrotizing lymphadenitis)Lymphadenopathy, fever, leukopeniaPosterior lymphadenopathy resolves in 3 monthsFNABRefer to hematology
Kimura diseaseEndemic in Asia; painless subcutaneous mass, eosinophiliaSubmandibular triangle, orbital, epicranial, periauricular; nontender, ill-definedEosinophilia, elevated immunoglobulin E level, biopsyRefer to hematology
Rosai-Dorfman diseaseOccasional fever in healthy young adultsMatted lymphadenopathyElevated erythrocyte sedimentation rate, polyclonal hypergammaglobulinemiaRefer to hematology
Systemic diseases
AmyloidosisAsymptomatic or associated CHF, nephrotic syndrome, neuropathyPainless systemic lymphadenopathyFNAB or excisional biopsyRefer to hematology
Sarcoidosis20- to 40-year-old black persons, variable presentation: persistent cough, skin rash/patch, joint pain, arrhythmiasPainless cervical, axillary, inguinal lymphadenopathyFNAB or excisional biopsy; chest radiography or CTRefer to pulmonary/rheumatology if necessary
Sjögren syndromeXerophthalmia, xerostomiaParotid gland enlargementAntinuclear antibodies, SS-A and SS-B antibodies, FNABSymptomatic treatment with sialagogues, frequent water intake
Chronic (usually evident as long-standing)
Carotid body tumorsFlushing, palpitations, hypertension if hormonally active, dysphagia, dyspnea, eustachian tube dysfunctionPainless oropharyngeal or upper anterior triangle of the neck; pulsatile, compressible with a bruit or thrill, mobile from medial to lateral directionCT, CT angiography (lyre sign); plasma and urine metanephrines, catecholaminesRefer to ENT
Congenital cysts
Branchial cleft cystOften diagnosed as a child; slow or rapidly growing after URI; acute or subacuteMandibular angle, anterior to sternocleidomastoidUltrasonographyAntibiotics; refer to ENT for excision after repeated infections
Dermoid cystChildren and young adultsSubmental triangle; soft, doughy, painlessCTSurgical excision
Thyroglossal duct cystOften diagnosed in childhood; slow growing or may arise quickly after URI; may present as acute or subacuteMidline, adjacent to the hyoid bone; rises with deglutitionCT (assures no thyroid cancer calcifications)Antibiotics; refer to ENT for excision after repeated infections
Glomus vagale, glomus jugulare tumorsFlushing, palpitations, hypertension if hormonally active, dysphagia, dyspnea, eustachian tube dysfunctionSimilar to carotid body tumors; ipsilateral tonsil may pulsate and be deviated to midlineCT, plasma and urine metanephrines, catecholaminesRefer to ENT
Goiters (enlarged thyroid)
Graves diseaseHyperthyroid symptomsAssociated exophthalmos, pretibial myxedemaTSH-receptor antibody; diffuse uptake on scintigraphyRadioactive iodine ablation, thyroidectomy, methimazole (Tapazole) or propylthiouracil
Hashimoto thyroiditisHypothyroid symptomsEnlarged thyroidThyroid peroxidase antibodyLevothyroxine
Iodine deficiencyReduced dietary iodine; exposure to thiocyanate (cassava, various vegetables)Diffusely enlarged thyroidDietary historyIncrease iodine/decrease thiocyanate containing compounds
Lithium useBipolar diseaseDiffusely enlarged thyroid/rare nodular thyroidHistory of exposureMonitor thyroid function at 6 to 12 months, treat dysfunction, discontinuation not required
Toxic multinodularHyperthyroid symptomsDiffusely nodularMultiple foci on scintigraphyRadioactive iodine ablation, thyroidectomy, methimazole or propylthiouracil
LaryngoceleRepetitive nose blowing, coughing, or blowing into a musical instrumentMidline, superior to thyroid cartilage; resonant, intermittent, globus sensationCT or laryngoscopyRefer to ENT
LipomasAge > 35 years, possible history of traumaSoft, mobile, discrete subcutaneous tumorsCTMonitor or excise
LiposarcomaMiddle-agedSlowly enlarging, painless, nonulcerated or rapidly growing and ulceratedCT; excisional biopsyExcision
Parathyroid cysts or cancerHypercalcemia symptoms, family history of multiple endocrine neoplasiaAnterior cervical triangleSerum calcium, parathyroid hormone immunoassayRefer to endocrinology, ENT
Thyroid nodules
Cold thyroid noduleUsually asymptomaticSolitary nodulesTSH, FT4, thyroid ultrasonography, FNAB if > 1 cmRefer to endocrinology, repeat ultrasonography in 6 to 18 months
Thyroid cancerRadiation, childhood lymphoma, family history, age < 45 years, hoarsenessSolitary nodulesTSH, FT4, thyroid ultrasonography, FNAB if > 1 cmRefer for excision
Toxic thyroid adenomaHyperthyroid symptomsSolitary nodulesTSH, FT4, thyroid ultrasonography, FNAB if > 1 cmRadioactive iodine or thyroidectomy