management of neck mases

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An Approach to Patients with a Neck Mass By Dr Alihussein kassam Intern doctor Mnazi mmoja hospital, zanzibar Thursday, June 16, 2022 copywrite@ Dr Alihussein Kassam 1

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Page 1: Management of neck mases

An Approach to Patients with a Neck Mass

By Dr Alihussein kassamIntern doctor

Mnazi mmoja hospital,zanzibar

Wednesday, May 3, 2023 copywrite@ Dr Alihussein Kassam 1

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Introduction

• Common clinical finding• All age groups• Very complex differential diagnosis• Systematic approach essential

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What will one think of?

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Anatomical Considerations• Prominent landmarks

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General Considerations

• Patient age– Pediatric (0 – 15 years): 90% benign– Young adult (16 – 40 years): similar to pediatric– Late adult (>40 years): “rule out CANCER”

• Location– Congenital masses: consistent in location– Metastatic masses: key to primary lesion

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Metastasis Location according to Various Primary Lesions

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Diagnostic Steps

• History

• Physical Examination

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Empirical Antibiotics

• Inflammatory mass suspected• Two week trial of antibiotics• Follow-up for further investigation

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Diagnostic Tests

• Fine needle aspiration biopsy (FNAB)

• Computed tomography (CT)

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Fine Needle Aspiration Biopsy

• Standard of diagnosis

• Indications

• Small gauge needle

• No contraindications (vascular ?)

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Fine Needle Aspiration Biopsy

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Computed Tomography

• Distinguish cystic from solid• Extent of lesion• Vascularity (with contrast)• Detection of unknown primary (metastatic)• Pathologic node (lucent, >1.5cm, loss of shape)

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Ultrasonography

Role of U/S is limited,

“Why do an ultrasound if you can palpate?”

Dr Naufal kassim

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Nodal Mass Workup in the Adult

• Any solid asymmetric mass MUST be considered a metastatic neoplastic lesion until proven otherwise

• Asymptomatic cervical mass – 12% of cancer• ~ 80% of these are SCCa

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Metastatic neck disease

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Metastatic neck disease

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Metastatic neck disease

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Primary Tumors

• Thyroid mass• Lymphoma• Salivary tumors• Lipoma

• Carotid body and glomus tumors

• Neurogenic tumors

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Thyroid Masses

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•Do all thyroids with a pathology enlarge?

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Lymphoma

• More common in children and young adults• Up to 80% of children with Hodgkin’s have a neck mass• Signs and symptoms– Lateral neck mass only (discrete, rubbery, nontender)– Fever– Hepatosplenomegaly– Diffuse adenopathy

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Lymphoma

• FNAB – first line diagnostic test• If suggestive of lymphoma – open biopsy• Full workup – CT scans of chest, abdomen, head and

neck; bone marrow biopsy

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Lymphoma

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Salivary Gland Tumors

• Enlarging mass anterior/inferior to ear or at the mandible angle is suspect

• Benign – Asymptomatic except for mass

• Malignant– Rapid growth, skin fixation, cranial nerve palsies

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Salivary Gland Tumors

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Carotid Body Tumor

Rare in childrenPulsatile, compressible massMobile medial/lateral not superior/inferiorClinical diagnosis, confirmed by angiogram or CTTreatment

Irradiation or close observation in the elderlySurgical resection for small tumors in young patientsHypotensive anesthesiaPreoperative measurement of catecholamines

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Carotid Body Tumor

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Lipoma

• Soft, ill-defined mass• Usually >35 years of age• Asymptomatic• Clinical diagnosis – confirmed by excision

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Lipoma

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Congenital and Developmental Mass• Epidermal and sebaceous cysts• Branchial cleft cysts• Thyroglossal duct cyst• Vascular tumors

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Epidermal and Sebaceous Cysts

• Most common congenital/developmental mass• Older age groups• Clinical diagnosis– Elevation and movement of overlying skin– Skin dimple or pore

• Excisional biopsy confirms

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Epidermal and Sebaceous Cysts

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Branchial Cleft Cysts

• Branchial cleft anomalies

• Present in older children or young adults often following URI

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Branchial Cleft Cysts

• Most common as smooth, fluctuant mass underlying the SCM

• Skin erythema and tenderness if infected• Treatment– Initial control of infection– Surgical excision, including tract

• May necessitate a total parotidectomy

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Branchial Cleft Cysts

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Thyroglossal Cyst

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Thyroglossal cyst

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Vascular Tumors

• Lymphangiomas and hemangiomas• Usually within 1st year of life• Hemangiomas often resolve spontaneously, while

lymphangiomas remain unchanged• CT/MRI may help define extent of disease

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Vascular Tumors (lymphangioma)

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Vascular Tumors (hemangioma)

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Vascular Tumors

• Treatment– Lymphangioma – surgical excision for easily accessible or

lesions affecting vital functions; recurrence is common– Hemangiomas – surgical excision reserved for those with

rapid growth involving vital structures or associated thrombocytopenia that fails medical therapy (steroids, interferon)

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Inflammatory Disorders

• Lymphadenitis• Granulomatous lymphadenitis

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Lymphadenitis

• Very common, especially within 1st decade• Tender node with signs of systemic infection• Directed antibiotic therapy with follow-up

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Lymphadenopathy

• Equivocal or suspicious FNAB in the pediatric nodal mass requires open excisional biopsy to rule out malignant or granulomatous disease

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Granulomatous lymphadenitis

• Infection develops over weeks to months• Minimal systemic complaints or findings• Common etiologies– TB, atypical TB, cat-scratch fever, actinomycosis,

sarcoidosis• Firm, relatively fixed node with injection of skin

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Granulomatous lymphadenitis• Typical M. tuberculosis– Usually responds to anti-TB medications– May require incisional biopsy for further workup– Chest X-ray ? Important?– Skin test?

• Symptoms– Low grade fever– Night sweats– >10% weight loss

• Signs– Persistence fistula following I & D

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Summary

• Extensive differential diagnosis• Age of patient is important• Accurate history and complete exam essential• FNAB – invaluable diagnostic tool• Possibility for malignancy in any age group• Close follow-up and aggressive approach is best for

favorable outcomes

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