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Table 1 Clinical and imaging characteristics of B cell indolent lymphomas undergoing histologic transformation

From: Multimodality imaging of indolent B cell lymphoma from diagnosis to transformation: what every radiologist should know

Subtype

Epidemiology

Clinical presentation

Imaging features

1/10 year risk of HT

FL

60 years old

Asymptomatic adenopathy (waxing and waning)

Multiple, deep non-obstructive adenopathy

3%/30%

M > F

Signs of extranodal involvement

Splenomegaly or focal splenic lesions

 
  

Extranodal involvement: organomegaly or focal lesions

 
  

Bone marrow, liver, lungs, CNS (more common)

 
  

Thyroid, parotid, breast, testis, skin (less common)

 
  

FDG avidity: 91–100%

 

CLL/SLL

71 years old

Asymptomatic lymphocytosisa

Adenopathy, splenomegaly,hepatomegaly

0.5–1%/16%

Increases with age

Peripheral adenopathy

Heterogeneous bone marrow infiltration (MRI)

Rare < 40 years old

Splenomegaly

Brain and meningeal enhancement (MRI)

 

Anemia, bleeding, infections (cytopenia)

FDG avidity: 73% (high avidity–shorter survival)

MZL

69 years old

  

0.5%/10%

MALT lymphoma

 

Organ specific symptoms

Adnexa oculi: enhancing issue infiltrating ocular appendages

 
 

Association:

Lung: lung nodules, consolidations, reticulation, peribronchial infiltrates

 
 

Helicobacter pylori infection

Gastrointestinal: smooth, polipoid or infiltrative lesions

 
 

Hashimoto thyroiditis

  
 

Clamydia Psittaci infection

  

Splenic MZL

 

Splenomegaly, cytopenia

Single or multiple focal splenic lesions or splenomegaly

 

Nodal MZL

 

Adenopathy

Adenopathy

 
   

FDG avidity: 49% (Ocular)–95% (Bronchial)

 

WM/LPL

60 years old

Recurrent infections, easy bruising

Bone marrow involvement (MRI)

0.5%/2.4%

 

Headache, Blurry vision

Diffuse: bones iso or hypointense to muscle

 
 

Neuropathy

Variegated: multiple enhancing foci in bone marrow

 
 

Organomegaly, adenopathy

+ Fractures

 
  

Lung, pleura, skin, liver involvement

 
  

CNS involvement (Bing-Neel syndrome)

 
  

T2 hyperintense hyperenhancing periventricular/subcortical foci

 
  

 Meningeal or spinal enhancement

 
  

Adenopathy

 
  

FDG avidity: 73%

 

NLPHL

Bimodal (childhood–4th decade)

Adenopathy

Adenopathy, splenomegaly, splenic lesions

0.73%/10%

Rare (500 cases/year in USA)

   
  1. HT histologic transformation, FL follicular lymphoma, CLL/SLL chronic lymphocytic leukemia/small lymphocytic lymphoma, MZL marginal zone lymphoma, MALT mucosa associated lymphoid tissue, WM/LPL Waldenstrom macroglobulinemia/lymphoplasmacytic lymphoma; NLPHL nodular lymphocyte-predominant Hodgkin lymphoma; CNS central nervous system
  2. aDefined as absolute lymphocyte count greater than 5000 cells/μL