Definition
About 3% of cases of anaplastic large cell lymphoma show a close resemblance to Hodgkin lymphoma1,2. The understanding is that this is not a true biological overlap but morphological mimicry. Diagnosis requires positivity for ALK1.
Although occurring across a wide age range, this variant of anaplastic large cell lymphoma is most common in children.
There is marked capsular fibrosis, with thick fibrous bands separating cellular nodules. Most of the neoplastic cells are mononuclear but with variable numbers of binucleate Reed-Sternberg like cells. Mummified and rare lacunar-like cells may be seen. The neoplastic cells may form cohesive sheets. In some cases they show a strong perivascular distribution, as seen in the small cell variant of ALCL. They may be seen within lymphatic sinuses. In cases with residual germinal centres, neoplastic cells show a perifollicular distribution. The background cells are lymphocytes and plasma cells, with most cases lacking substantial numbers of eosinophils or neutrophils. Some histiocytes may be present but granulomata are lacking.
The neoplastic cells may be of T or null immunophenotype.
3/71 |
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4/101 |
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4/71 |
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4/71 |
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2/71 |
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0/71 |
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0/101 |
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0/101 |
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6/91 |
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9/91 |
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Perforin |
8/81 |
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EBV / LMP-1 |
0/81 |
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0/61 |
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BNH9 |
4/61 |
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Hodgkin lymphoma, particularly nodular sclerosing type II: the possibility of ALCL resembling Hodgkin lymphoma should be considered in cases with neoplastic cells strongly positive for EMA or positive for T-cell markers (Hodgkin lymphoma may show cytoplasmic dot-like positivity for CD3)
Atypical T-cell lymphoma, e.g. nodal cytotoxic T-cell lymphoma.
This page last revised 9.4.2006.
©SMUHT/PW Bishop