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Guidelines on Diagnosis and Treatment of Malignant Lymphomas

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Pathologic <strong>Diagnosis</strong><br />

<strong>of</strong> Lymphoma<br />

General comments<br />

1. Primary diagnosis<br />

a. Complete lymph node excisi<strong>on</strong> in the presence <strong>of</strong> nodal<br />

disease is the optimum diagnostic material <strong>and</strong> should be<br />

utilised wherever possible. *<br />

b. The complete lymph node excisi<strong>on</strong> should be transported<br />

immediately in a fresh state to the laboratory.<br />

c. The fresh lymph node should be h<strong>and</strong>led as per algorithm<br />

<strong>on</strong> page 15.<br />

d. *Where full lymph node excisi<strong>on</strong> is not possible e.g.<br />

inaccessible mass or extranodal disease, core biopsy is the<br />

next best opti<strong>on</strong> for accurate primary diagnosis unless a<br />

resecti<strong>on</strong> has been or will be undertaken. Multiple large<br />

cores should ideally be submitted fresh to the laboratory <strong>on</strong><br />

saline soaked gauze otherwise they should be submitted in<br />

10% buffered formalin.<br />

e. All cases must be received with relevant clinical informati<strong>on</strong>.<br />

2. The role <strong>of</strong> Flow Cytometry (FCM)<br />

a. FCM is useful for accurate diagnosis in all small cell /<br />

follicular pattern lesi<strong>on</strong>s.<br />

b. FCM <strong>on</strong> aspirated material may provide a reas<strong>on</strong>able<br />

alternative to biopsy in recurrent disease where tissue is<br />

not easily obtainable e.g. elderly/frail patient, inaccessible<br />

site. Such FNA samples require co-ordinati<strong>on</strong> with the<br />

laboratory as special fixati<strong>on</strong> (RPMI) <strong>and</strong> immediate<br />

processing is required<br />

3. Optimum h<strong>and</strong>ling <strong>of</strong> fresh lymph node excisi<strong>on</strong><br />

a. Ensure immediate transfer from the theatre to laboratory.<br />

b. Bisect node <strong>and</strong> perform touch preparati<strong>on</strong>s.<br />

i. Air dried x 2 – Giemsa stain<br />

ii. Air dried X6-8 FISH studies if required<br />

iii. Fixed x 2 – H & E stain<br />

c. Sample porti<strong>on</strong> <strong>of</strong> tissue for:<br />

i. Freezing – 1 porti<strong>on</strong> in “RNA later”, 1 porti<strong>on</strong> fresh<br />

frozen (this will preserve material for molecular study<br />

should this be required).<br />

ii. RPMI for FCM (this will preserve the cells <strong>and</strong> allow<br />

transport to nearest centre <strong>of</strong>fering FCM <strong>and</strong>/or<br />

Cytogenetics service).<br />

iii. Formalin for routine fixati<strong>on</strong> <strong>and</strong> processing.<br />

4. Classificati<strong>on</strong> <strong>and</strong> grading<br />

a. Use WHO classificati<strong>on</strong> 4th editi<strong>on</strong> 2008<br />

b. Where applicable use WHO grading e.g.<br />

Follicular Lymphoma (see page 29)<br />

5. The role <strong>of</strong> FCM/Cytogenetics/<br />

Gene expressi<strong>on</strong> pr<strong>of</strong>iling<br />

Material should be preserved in RPMI <strong>and</strong> frozen<br />

for availability for cytogenetic analysis <strong>and</strong> other<br />

relevant evaluati<strong>on</strong><br />

6

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