This lymph node from a 77-year-old woman with suspected metastatic tonsil cancer showed a diffuse proliferation (panel A: hematoxylin and eosin [H&E] stain, original magnification ×100) of small- to medium-sized mature lymphoid cells with scant cytoplasm (panel B: Giemsa stain, original magnification ×400), intermixed with prolymphocytes and paraimmunoblasts (panel B inset: Giemsa stain, original magnification ×640) in proliferation centers. Areas of coagulation necrosis (panel C: H&E stain, original magnification ×100) contained cells with eosinophilic nuclear inclusions intermixed with debris and granulocytes (panel D: H&E stain, original magnification ×800). The lymphoid cells expressed CD20, CD5, LEF1, and, focally, CD23, consistent with a diagnosis of small lymphocytic leukemia (SLL); showed increased proliferation (panel E: MIB1 stain, original magnification ×200); showed strong positivity for p53 (panel F: P53 stain, original magnification ×200) with confirmed TP53 mutation; and interspersed Epstein-Barr virus (EBV)+ and LMP1+ cells (panel G: EBV-encoded small RNAs in situ hybridization, original magnification ×100). The nuclear inclusions in the necrosis were positive for herpes simplex virus (HSV) (panel H: HSV I and II stain, original magnification ×200).
This case highlights the propensity for local reactivation of latent viral infections in the background of chronic lymphocytic leukemia (CLL)/SLL, due to immune dysregulation even in untreated patients. Neoplastic B cells in CLL act as HSV antigen-presenting cells and are readily infected. HSV lymphadenitis is an exceedingly rare finding, but characteristically shows rapid lymph node enlargement and is an important differential diagnosis for Richter transformation, recommending a low threshold for HSV staining in the setting of necrosis.
This lymph node from a 77-year-old woman with suspected metastatic tonsil cancer showed a diffuse proliferation (panel A: hematoxylin and eosin [H&E] stain, original magnification ×100) of small- to medium-sized mature lymphoid cells with scant cytoplasm (panel B: Giemsa stain, original magnification ×400), intermixed with prolymphocytes and paraimmunoblasts (panel B inset: Giemsa stain, original magnification ×640) in proliferation centers. Areas of coagulation necrosis (panel C: H&E stain, original magnification ×100) contained cells with eosinophilic nuclear inclusions intermixed with debris and granulocytes (panel D: H&E stain, original magnification ×800). The lymphoid cells expressed CD20, CD5, LEF1, and, focally, CD23, consistent with a diagnosis of small lymphocytic leukemia (SLL); showed increased proliferation (panel E: MIB1 stain, original magnification ×200); showed strong positivity for p53 (panel F: P53 stain, original magnification ×200) with confirmed TP53 mutation; and interspersed Epstein-Barr virus (EBV)+ and LMP1+ cells (panel G: EBV-encoded small RNAs in situ hybridization, original magnification ×100). The nuclear inclusions in the necrosis were positive for herpes simplex virus (HSV) (panel H: HSV I and II stain, original magnification ×200).
This case highlights the propensity for local reactivation of latent viral infections in the background of chronic lymphocytic leukemia (CLL)/SLL, due to immune dysregulation even in untreated patients. Neoplastic B cells in CLL act as HSV antigen-presenting cells and are readily infected. HSV lymphadenitis is an exceedingly rare finding, but characteristically shows rapid lymph node enlargement and is an important differential diagnosis for Richter transformation, recommending a low threshold for HSV staining in the setting of necrosis.
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![This lymph node from a 77-year-old woman with suspected metastatic tonsil cancer showed a diffuse proliferation (panel A: hematoxylin and eosin [H&E] stain, original magnification ×100) of small- to medium-sized mature lymphoid cells with scant cytoplasm (panel B: Giemsa stain, original magnification ×400), intermixed with prolymphocytes and paraimmunoblasts (panel B inset: Giemsa stain, original magnification ×640) in proliferation centers. Areas of coagulation necrosis (panel C: H&E stain, original magnification ×100) contained cells with eosinophilic nuclear inclusions intermixed with debris and granulocytes (panel D: H&E stain, original magnification ×800). The lymphoid cells expressed CD20, CD5, LEF1, and, focally, CD23, consistent with a diagnosis of small lymphocytic leukemia (SLL); showed increased proliferation (panel E: MIB1 stain, original magnification ×200); showed strong positivity for p53 (panel F: P53 stain, original magnification ×200) with confirmed TP53 mutation; and interspersed Epstein-Barr virus (EBV)+ and LMP1+ cells (panel G: EBV-encoded small RNAs in situ hybridization, original magnification ×100). The nuclear inclusions in the necrosis were positive for herpes simplex virus (HSV) (panel H: HSV I and II stain, original magnification ×200).](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/136/26/10.1182_blood.2020008950/1/m_bloodbld2020008950f1.png?Expires=1765135566&Signature=j-cPfkvuP14YIyWV0UQ6ogf9jEe415pVfcSrUfYL0eJuLlU6bUKVyAYaNylRJA62fVogHxOjOi6xpE2HOnfkh0ES~sd0IXQtRJBA5-RgLwU213cJc9TeVZViB8xwB3D0G-qet8Sc0xaqXhSCW~Krt8FlTewegrJ7ZZh1SCnyRLWfnQIfe0-KpbVa8Hg8fQcPu-vT4nxdw3SDWVTQgzxS3-dNLxY1tuTg7t0Qkv7rubYGm56FoOrIX7ovkuAjzhvjCy9WHBq3weo19fQznGQmtlG0k4txdRJFxigF7XGxQUwSE2mLLtgMPAm~l51LJHxN8bEnfm3dWYzfRthOO4lStw__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)
![This lymph node from a 77-year-old woman with suspected metastatic tonsil cancer showed a diffuse proliferation (panel A: hematoxylin and eosin [H&E] stain, original magnification ×100) of small- to medium-sized mature lymphoid cells with scant cytoplasm (panel B: Giemsa stain, original magnification ×400), intermixed with prolymphocytes and paraimmunoblasts (panel B inset: Giemsa stain, original magnification ×640) in proliferation centers. Areas of coagulation necrosis (panel C: H&E stain, original magnification ×100) contained cells with eosinophilic nuclear inclusions intermixed with debris and granulocytes (panel D: H&E stain, original magnification ×800). The lymphoid cells expressed CD20, CD5, LEF1, and, focally, CD23, consistent with a diagnosis of small lymphocytic leukemia (SLL); showed increased proliferation (panel E: MIB1 stain, original magnification ×200); showed strong positivity for p53 (panel F: P53 stain, original magnification ×200) with confirmed TP53 mutation; and interspersed Epstein-Barr virus (EBV)+ and LMP1+ cells (panel G: EBV-encoded small RNAs in situ hybridization, original magnification ×100). The nuclear inclusions in the necrosis were positive for herpes simplex virus (HSV) (panel H: HSV I and II stain, original magnification ×200).](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/136/26/10.1182_blood.2020008950/1/m_bloodbld2020008950f1.png?Expires=1765135567&Signature=wzRa~CJ3N1uizN6rn4Q7KlSyY4X~rxtAxDC~PIVI7h-zcRTKlw3WU6tDx5lNkOuiYTtYJ9jSjNow2fsm33b9VcxGOczQlAhbAVL~Pj7bcNydsY41k8K0erO7GQuO~zSVFAyGo9eF4x45dFgkWe9V-R68OjtZjZhrYF9F1mwCx271ogUlSbYcFYMpllpfNaheTNL21YmG-5wyO7Hz~9ef~cSjQjQ8m2lkM9fISWDdxr4X-RO~NlBNdYUdrDxI7sGSxwi49bCpxWVW-wZxrRXI3Wv36PDizDPL0DN5Hq1tNMhjnS9NqrgcCLg7rsxk3gwVgP7Edjx05mj8QJq~KomIxw__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)