Changes

no edit summary
Line 1: Line 1:  +
{{DISPLAYTITLE:Nodular Sclerosis Classic Hodgkin Lymphoma}}
 +
 +
 +
<blockquote class='blockedit'>{{Box-round|title=PREVIOUS EDITION|This page from the 4th edition of Haematolymphoid Tumours is being updated. See 5th edition [[HAEM5:Table_of_Contents|Table of Contents]].
 +
}}</blockquote>
 
==Primary Author(s)*==
 
==Primary Author(s)*==
   Line 7: Line 12:  
==Cancer Category/Type==
 
==Cancer Category/Type==
   −
[[Classic Hodgkin Lymphoma]]
+
[[HAEM4:Classic Hodgkin Lymphoma]]
    
==Cancer Sub-Classification / Subtype==
 
==Cancer Sub-Classification / Subtype==
Line 15: Line 20:  
==Definition / Description of Disease==
 
==Definition / Description of Disease==
   −
Hodgkin lymphomas (HL) are a group of B-cell neoplasms that arise in lymph nodes, categorized mainly into nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) and classic Hodgkin lymphoma (CHL). CHL accounts for approximately 90% of HL and is subdivided into four histologic types, [[Nodular Sclerosis Classic Hodgkin Lymphoma|nodular sclerosis CHL (NSCHL)]], [[Lymphocyte-Rich Classic Hodgkin Lymphoma|lymphocyte-rich CHL]], [[Mixed Cellularity Classic Hodgkin Lymphoma|mixed cellularity CHL]], and [[Lymphocyte-Depleted Classic Hodgkin Lymphoma|lymphocyte-depleted CHL]]. NSCHL is the most common type of CHL and is characterized by the appearance of nodular growth surrounded by prominent collagen bands and the presence of lacunar type Hodgkin/Reed-Sternberg cells (HRS).  
+
Hodgkin lymphomas (HL) are a group of B-cell neoplasms that arise in lymph nodes, categorized mainly into nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) and classic Hodgkin lymphoma (CHL). CHL accounts for approximately 90% of HL and is subdivided into four histologic types, [[HAEM5:Classic Hodgkin lymphoma|nodular sclerosis CHL (NSCHL)]], [[HAEM5:Classic Hodgkin lymphoma|lymphocyte-rich CHL]], [[HAEM5:Classic Hodgkin lymphoma|mixed cellularity CHL]], and [[HAEM5:Classic Hodgkin lymphoma|lymphocyte-depleted CHL]]. NSCHL is the most common type of CHL and is characterized by the appearance of nodular growth surrounded by prominent collagen bands and the presence of lacunar type Hodgkin/Reed-Sternberg cells (HRS).  
    
==Synonyms / Terminology==
 
==Synonyms / Terminology==
Line 214: Line 219:  
==Links==
 
==Links==
   −
[[Hodgkin Lymphomas|Hodgkin Lymphoma]]
+
[[HAEM4:Hodgkin Lymphomas|Hodgkin Lymphoma]]
   −
[[Classic Hodgkin Lymphoma]]
+
[[HAEM4:Classic Hodgkin Lymphoma]]
   −
[[Nodular Sclerosis Classic Hodgkin Lymphoma|Nodular sclerosis CHL]]
+
[[HAEM5:Classic Hodgkin lymphoma|Nodular sclerosis CHL]]
   −
[[Lymphocyte-Rich Classic Hodgkin Lymphoma|Lymphocyte-rich CHL]]
+
[[HAEM5:Classic Hodgkin lymphoma|Lymphocyte-rich CHL]]
   −
[[Mixed Cellularity Classic Hodgkin Lymphoma|Mixed cellularity CHL]]
+
[[HAEM5:Classic Hodgkin lymphoma|Mixed cellularity CHL]]
   −
[[Lymphocyte-Depleted Classic Hodgkin Lymphoma|Lymphocyte-depleted CHL]]
+
[[HAEM5:Classic Hodgkin lymphoma|Lymphocyte-depleted CHL]]
    
<br />
 
<br />
Line 233: Line 238:  
==Notes==
 
==Notes==
 
<nowiki>*</nowiki>Primary authors will typically be those that initially create and complete the content of a page.  If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage).  Additional global feedback or concerns are also welcome.
 
<nowiki>*</nowiki>Primary authors will typically be those that initially create and complete the content of a page.  If a subsequent user modifies the content and feels the effort put forth is of high enough significance to warrant listing in the authorship section, please contact the CCGA coordinators (contact information provided on the homepage).  Additional global feedback or concerns are also welcome.
 +
[[Category:HAEM4]] [[Category:DISEASE]]