Morphological markers
A key feature of the disease is Reed—Sternberg cells. These are large elements with a characteristic structure:
- "Owl-eye" appearance: two symmetric nuclei with large eosinophilic nucleoli surrounded by a clear halo.
- Amphophilic cytoplasm: stains with both acidic and basic dyes.
- Pyroninophilia: high RNA concentration makes the cytoplasm sensitive to pyronin stains.
Specific forms also exist: Hodgkin cells (mononuclear), lacunar cells (with vacuoles), and L- and H-type cells ("popcorn cells").
Reactive microenvironment
The tumor process is accompanied by a pronounced reaction of the surrounding tissues. The lymph node exhibits:
- Complete disappearance of normal follicles.
- Disruption of node architectonics.
- Polymorphic cellular infiltrate including lymphocytes, plasmocytes, histiocytes, eosinophils, and neutrophils.
- Development of varying degrees of fibrosis.
Prognosis and survival
Treatment success directly depends on the timeliness of therapy. With an adequate approach, 5-year survival in early stages (I–II) approaches 100%, whereas in stage IV it is about 50%. The main causes of adverse outcomes remain disease progression and complications from aggressive treatment.
Briefly: answers to topical questions
What histological variants of lymphogranulomatosis are distinguished in the modern morphological classification?
The modern WHO classification distinguishes two main types of Hodgkin's lymphoma: classical and nodular lymphocyte-predominant.
Histological variants of classical Hodgkin's lymphoma:
- Nodular sclerosis variant — includes types I and II.
- Mixed cellularity variant.
- Lymphocyte-rich classical variant (lymphocyte-rich) — corresponds to the outdated term "lymphocytic predominance".
- Lymphocyte-depleted variant — is rare.
Nodular lymphocyte-predominant Hodgkin's lymphoma is distinguished as a separate type with a different pathogenesis and immunophenotype.
What does the spleen look like macroscopically in lymphogranulomatosis?
Macroscopically, lymphogranulomatosis forms the so-called "porphyry spleen". The spleen is enlarged and firm. On cross-section, red pulp is seen with white-yellow foci and streaks.
In which organs are extranodal lesions and metastases most frequently detected during the generalization of lymphogranulomatosis?
During the generalization of lymphogranulomatosis, the spleen, liver, lungs, bone marrow, stomach and other parts of the gastrointestinal tract, skin, and kidneys may be involved. Sources also indicate that primary extranodal localization in the spleen, liver, lungs, stomach, skin, and bone marrow is rare.
What pathological processes and complications are most often the direct cause of death in patients with lymphogranulomatosis?
The direct causes of death in patients with lymphogranulomatosis are most often progression of the underlying disease and complications of ongoing therapy.
Main pathological processes and complications:
- Disease progression — generalization of the process with involvement of internal organs, development of cachexia, and multiple organ failure.
- Chemotherapy and radiotherapy complications — toxic effects on organs, development of secondary tumors.
- Infectious complications — sepsis, septic shock, and pneumonia against the background of secondary immunodeficiency.
- Critical conditions — acute respiratory failure, acute kidney injury, cerebrovascular accidents, gastrointestinal bleeding, and tumor lysis syndrome.
"Owl in a lacuna": if you see a cell with two eye-like nuclei (Reed—Sternberg) or a cell in an empty space (lacunar) — it is lymphogranulomatosis.
Class and exam questions
Why are Reed—Sternberg cells called "owl eyes"?
Due to the presence of two symmetric nuclei with large nucleoli, which visually resemble an owl's eyes.
What is the role of the Epstein—Barr virus in pathogenesis?
The virus genome is detected in tumor cells in 70% of patients, indicating its involvement in the cell transformation process.
What is the diagnostic value of Hodgkin cells?
They are mononuclear variants of Reed—Sternberg cells and help identify tumor metastases in the liver and bone marrow.
What else to study on this topic
- Immunophenotypic differences between lymphoma variants.
- Mechanisms of NF-κB factor activation in EBV-negative cases.
- Differential diagnosis with other types of lymphomas.
- Genetic mutations characteristic of germinal center cells.
Master the entire topic in the "Pathological Anatomy" course
This is a summary. The course covers everything tested in classes and exams.
- Complete study guide on "Lymphogranulomatosis" and 4,414 more pages of the subject
- Assignments and quizzes after every topic — just like in a colloquium
- AI tutor answers questions on the topic anytime
- 153 video lessons on the subject
Other topics in Hematopoietic System Diseases
Free video lessons: pathological anatomyShort lessons with study notes — no registration required.
Prepared by WhiteCoat Pro faculty in accordance with the medical school curriculum. For educational purposes only.