Lymphocyte depleted Hodgkin lymphoma, intrapelv lymph nodes

This code signifies a rare and aggressive subtype of Hodgkin lymphoma characterized by a paucity of lymphocytes and a high proportion of Reed-Sternberg cells, specifically affecting the lymph nodes located within the pelvic region. This form of Hodgkin lymphoma typically presents with more advanced disease and a poorer prognosis compared to other subtypes.

Use this code when documentation explicitly states a diagnosis of lymphocyte-depleted Hodgkin lymphoma with primary or metastatic involvement of intrapelvic lymph nodes. This diagnosis is typically confirmed through biopsy and histopathological examination. Supporting documentation should clearly specify both the subtype of Hodgkin lymphoma and the anatomical location.

• Ensure the pathology report explicitly confirms "lymphocyte depleted" subtype and "intrapelvic lymph nodes" involvement.
• Do not confuse with other Hodgkin lymphoma subtypes (e.g., nodular sclerosis, mixed cellularity) or other extranodal sites.
• Sequence this code as the primary diagnosis when it is the reason for the encounter, followed by any associated signs, symptoms, or complications.