Lymphatics And Lymph Node Enlargement
Question.1. Enumerate the causes of lymph node enlargement in neck, describe the clinical features and management of tubercular lymphadenitis.
Or
Write in brief about clinical features and management of tuberculous lymphadenitis.
Or
Describe the clinical features and treatment of tubercular sinus in neck.
Or
Write in brief management of tubercular cervical lymphadenopathy.
Answer.
Causes of Enlargement of Lymph Node in Neck
1. Inflammatory: due to microorganism.
- Bacterial as: Streptococcus, Mycobacterium, Treponema pallidum, Actinomycosis.
- Viral as: Lymphogranuloma venereum, Infectious mononucleosis, HIV
- Parasite as: Wuchereria bancrofti
- Fungus as: Blastomycosis.
2. Lymphatic leukemia.
3. Autoimmune disorders:
- Systemic lupus erythematous
- Rheumatoid arthritis
- Sclerosis.
4. Neoplasms: Malignant neoplasm involves lymph node like.
- Malignant lymphoma
- Hodgkin’s disease
- Lymphosarcoma
- Malignant melanoma.
5. Secondaries in lymph nodes.
Read And Learn More: General Surgery Question And Answers
Clinical Features of Tubercular Lymphadenitis
- Swelling in the neck is present, which is fim and mattd.
- Cold abscess is soft, smooth, non-tender, flctuant, without involvement of the skin. It is not warm.
- As a result of increased pressure, cold abscess ruptures out of the deep fascia to form collar stud abscess which is adherent to the overlying skin.
- Once collar stud abscess bursts open, discharging sinus is formed. It can be multiple, wide open mouth, often undermined, non-mobile with bluish color around the edge. It is usually not indurated.
- Tonsils may be studded with tubercles and so clinically should always be examined.
- Associated pulmonary tuberculosis should also be looked for. In 20% cases of tuberculous lymphadenitis, there may be associated pulmonary tuberculosis or it may be a primary focus.
- Cervical spine is examined for tuberculosis.
- Axillary nodes, when involved are due to retrograde lymphatic spread from neck nodes or blood spread.
- Inguinal lymph nodes are involved occasionally through blood.
- Bluish hyperpigmented involved overlying skin is called as scrofuloderma.
- Tuberculous pus with caseating cheesy creamy material is infective as it contains multiplying organisms.
- Atypical mycobacterial tuberculosis can occur occasionally.
- Such disease may be resistant to drug therapy.
- Sinus may persist due to firosis, calcifiation, secondary infection inadequate reach of drug tomaintain optimum concentration in caseation
Management of Tubercular Lymphadenitis
Drugs:
Antitubercular drugs have to be started:
- Rifampicin 450 mg OD on empty stomach. It is bactericidal.
- INH: 300 mg OD. It is bactericidal.
- Ethambutol 800 mg OD. It is bacteriostatic.
- Pyrazinamide 1500 mg OD (or 750 mg BD). It is bactericidal.
Duration of treatment is usually 6–9 months.
Aspiration: When there is cold abscess, initially it is aspirated. Wide bore needle is introduced into the cold abscess in a nondependent site along a “Z” track (in zigzag pathway) so as to prevent sinus formation.
Incision and drainage: Ifcold abscess recurs, then it should be drained. Drainage is done through a nondependent incision. After draining the caseating material, wound is closed without placing a drain.
Surgical removal: Surgical removal of tubercular lymph nodes are indicated when
- There is no local response to drugs
- When sinus persists.
It is done by raising skin flps and removing all caseating material and lymph nodes. Care is taken not to injure major structures.
Excision of the sinus tract is often essential when sinus develops.
Question.2. Write in brief about etiology, pathology, clinical features and treatment of Cervical Tuberculous Lymphadenitis.
Or
Discuss etiology, pathology, clinical features and treatment of Tuberculous Lymphadenitis.
Answer.
Cervical Tuberculous Lymphadenitis Etiology
- Tuberculous bacillus, i.e. Mycobacterium tuberculosis is the bacteria which leads to tuberculosis.
- Disease is caused in people of low socioeconomic status, unhygienic living conditions and malnutrition.
- In 20% of cases, lymph nodes are affcted in posterior triangle due to involvement of adenoid.
Cervical Tuberculous Lymphadenitis Pathology
When the tubercle bacilli are introduced into the tissue.
- The initial response of neutrophils
- There is progressive infitration by macrophages
- Macrophages start phagocytosing the tubercle bacilli.
- Activated CD4 + T-cells develop.
- In 2 to 3 days, the macrophages undergo structural changes and form epithelioid cells.
- The epithelioid cells aggregated into tight clusters or granulomas.
- Some macrophages form multinucleated giant cells.
- Hard tubercles form by the mass of epithelioid cells and the giant cells in a zone of lymphocytes,plasma cells and firoblasts.
- Center of the cellular mass undergoes caseous necrosis,characterized by cheesy appearance called as soft tubercle.
Question.3. Write short note on Tuberculous Lymphadenitis.
Or
Discuss briefly Tuberculous Lymphadenitis.
Or
Write brief notes on Tuberculous Lymphadenitis.
Or
Write in brief about Tubercular Cervical Lymphadenitis.
Answer. Tubercular lymphadenitis is defied as chronic specific granulomatous inflammation with caseation necrosis of lymph node.
Tuberculous Lymphadenitis Staging
Stage of lymphadenitis
- Common in young adult between 20–30 years.
- Upper anterior deep cervical nodes are enlarged.
- Non-tender, discrete, mobile, fim lymph node is palpable.
Stage of Matting
- Results due to involvement of capsule of lymph node.
- Nodes moves together
- Firm, non-tender.
Stage of Cold abscess
- It occurs due to caseation necrosis of lymph node.
- No local rise in temperature.
- No tenderness.
- No redness.
- Soft, cystic and flctuant swelling.
- Transillumination is negative.
- On sternomastoid contraction test, it becomes less prominent indicating that it is deep-to-deep fascia.
Stage of Collar Stud abscess
It results when a cold abscess rupture through the deep fascia and form another swelling in the subcutaneous plane which is flctuant.
Stage of Sinus
- Collar stud abscess burst and form tubercular sinus.
- Common in young female.
- It can be multiple.
- Resemble an ulcer with undermined edge.
- No indurations.
- Skin surrounding the sinus shows pigmentation and sometimes bluish in color.
Tuberculous Lymphadenitis Differential Diagnosis
- Non-specific lymphadenitis
- Secondaries in neck
- Lymphomas and chronic lymphatic leukemia
- Branchial cyst and lymphatic cyst mimic cold abscess
- HIV with lymph node involvement
Tuberculous Lymphadenitis Investigations
- Hematocrit, ESR, peripheral smear.
- FNAC oflymph node and smear forAFB and culture: FNAC is very useful but not as superior as open node biopsy.
False negative, false positive results and altering the node architecture, and so eventual need of open biopsy are the problems.
Epithelioid cells (modifid histiocytes/macrophages) are diagnostic.
Langhans giant cells, lymphocytes, plasma cells are other features. - Open biopsy: Open biopsy is more reliable for tuberculosis (and also in lymphoma; but it is contraindicated in node secondaries); entire node ideally two nodes if possible has to be taken intact; one in formalin for pathology, other in normal saline for microbiology (AFB).
- HIV test (ELISA and western blot).
- Lowenstein-Jensen media is used for culture which takes 6 weeks to give result; so selenite media is often used which shows growth in 5 days.
- Mantoux test may be useful; but not very reliable.
- Chest X-ray to look for pulmonary tuberculosis.
- Polymerase chain reaction (PCR) is very useful method.
Question.4. Write short note on: Collar Stud Abscess.
Answer. Collar stud abscess is an acute suppurative infection of a digit which present stud-like blister.
- It is bilocular abscess with one lobule deep to the deep fascia and another lobule is superfiial to fascia.
Both the locule intercommunicates with each other through a small perforation in the deep fascia.
Such an abscess can occur anywhere in the body.
Collar Stud Abscess Types
- Pyogenic: When pyogenic abscess develops deep to deep fascia and gradually pressure mouth so that the deep fascia perforates, the pus comes out into superfiial fascia.
So, pyogenic collar stud abscess is more commonly seen in hand where deep fascia is in the palmer fascia. - Tuberculous: This is more often seen in the neck from caseation tubercular lymph node.
The cold abscess beneath the deep fascia ruptures and forms another swelling in subcutaneous plane which is fluctuant. It remains adhere to skin.
Collar Stud Abscess Treatment
Pyogenic Collar Stud abscess
- Drainage ofterminal pulp space byanoblique deep incision.
- Systemic antibiotics should be given.
Tuberculous Collar Stud Abscess
It should be treated like as cold abscess, i.e.
- Anti-tubercular treatment is given.
- Zig-zag aspiration by wide bore needle in non-dependent area for prevention of sinus perforation.
- Drainage can be done by using non-dependent incision and later on closure of wound is done without placing a drain
Question.5. Describe the causes of generalized lymphadenopathy and management of Hodgkin’s lymphoma.
Answer. Enlargement of lymph gland is called as lymphadenopathy.
Causes of Generalized Lymphadenopathy
- Acute infection process: Glandular fever.
- Tuberculosis
- Syphilis: In secondary stage
- Disseminated lupus erythematosus
- Blood disease: Acute lymphatic leukemia, chronic lymphatic leukemia
- Neoplasm: Secondary carcinoma
- HIV infection and AIDS
- Sarcoidosis.
Management of Hodgkin’s Lymphoma Stage I and II:
- Mainly radiotherapy, i.e. external high cobalt radiotherapy
- Above the diaphragm: Y-fild therapy, covering cervical,axillary, mediastinal lymph nodes.
- Below the diaphragm: Mantle or inverted-Y fild therapy covering para-aortic and iliac nodes.
- Chemotherapy is also given.
Management of Hodgkin’s Lymphoma Stage III and IV:
- In this, mainly chemotherapy is given.
- Regimens used are:
MoPP regimen
- Mechlorethamine: 6 mg/sqm on 1st and 8th day
- Oncovine: 1.4 mg/sqm on 1st and 10th day
- Procarbazine: 100 mg orally daily for 10 days
- Prednisolone: 45 mg orally daily for 10 days
MOPP combination is given in 6 courses with no drugs given from 15th to 28th day.
ABVd Regimen
- Adriamycin: 30 mg/sqm
- Bleomycin: 10 mg/sqm
- Vinblastine: 6 mg/sqm
- Dacarbazine: 350 mg/sqm
The cycle is repeated on 20th day.
Splenectomy is done in many patients except with stage IV disease.
Question.6. Write in brief Cold Abscess in Neck.
Or
Write short note on cold abscess in neck.
Or
Describe diagnostic features and treatment of cold abscess.
Answer. Cold abscess is common in neck.
Cold Abscess in Neck Etiology
- Tuberculous lymphadenitis: Cold abscess is seen commonly in anterior triangle of neck
- Tuberculosis ofcervical spine: Cold abscess is seen commonly in posterior triangle of neck.
Cold Abscess in Neck Clinical Features
- It is commonly seen in young individuals but can occur in any age group.
- Swelling in neck is smooth, non-tender, soft, flctuating,non-transilluminant, non-mobile and is notadherentto skin.
- There is presence of neck pain, neck rigidity and restricted movements of cervical spine.
- Rust sign: With change in position and often when patient is seated, he support his head with hands and forearm.
- There is presence of evening fever, loss of weight and appetite.
- Mattd lymph nodes adjacent to cold abscess should be palpable.
Cold Abscess in Neck Diagnostic Features
- Oral cavity, chest and tonsils of the patient are thoroughly examined.
- ESR is raised
- Mantoux test is positive. This test is useful but not reliable.
- Presence of anemia and lymphocytosis
- Chest X-ray show pulmonary tuberculosis
- FNAC of cold abscess under microscopic examination show epithelioid cells.
- Fluid obtained by FNAC should be stained by ZiehlNeelsen stain which reveals acid-fast bacilli
- X-ray neck is done in cervical spine tuberculosis to identify reduced joint space, vertebral destruction, soft tissue shadow.
- MRI of cervical spine, ultrasonography or CT scan neck are needed to confim anatomical location and number of lesions.
Cold Abscess in Neck Treatment
- Anti-tubercular treatment is given to the patient.
- Non-dependent aspiration of cold abscess.
- Diseased neck nodes should be excised.
- Immobilization of cervical spine by plaster jacket/collar for 4 months.
Cervical spine fusion by open surgical method,if diseased spine is unstable.
Question.7. Write short note on Lymphoedema.
Answer. Lymphoedema is the accumulation of lymph in extracellular and extravascular fluid compartment commonly in subcutaneous tissue.
It is due to defective lymphatic drainage.
Lymphoedema Classification
Primary without any identifible lymphatic disease.
Secondary is acquired.
Lymphoedema Pathophysiology
Decreased lymphatic contractility, lymphatic valvular insuffiency, lymphatic obliteration by infection, tumor or surgery causes all effcts and pathology of lymphoedema.
This leads to lymphatic hypertension and dilatation causing lymph stasis, accumulation of proteins, glycosamines, growth factors,and bacteria.
There is more collagen formation, deposition of proteins, fibroblasts, ground substance causing firosis in subcutaneous and outside deep fascia.
Muscles are normal without any edema but may get hypertrophied.
Lymphoedema Clinical Features
- Most commonly lower limb is involved.
- Presence of swelling in the foot which extends progres sively in the neck and show tree-trunk pattrn leg.
- Presence of bufflo hump in dorsum of foot.
- Athlete’s foot with joint pain and disability
- Fever, malaise and headache
- Initially pitting edema occurs which later on become
- Non-Pittng.
- Stemmer’s sign is positive, i.e. skin over dorsum of foot cannot be pinched because of subcutaneous firosis.
Lymphoedema Grading of lymphoedema
This is given by Brunner
- Latent: No clinically apparent lymphoedema
- Grade I: Pittng edema which more or less disappears on elevation of the limb.
- Grade II: Non-pittng edema occur which does not reduce on elevation
- Grade III: Edema with irreversible skin changes like firosis,papillae, fisuring.
Lymphoedema Treatment
Conservative:
- Elevation of limb, exercise and weight reduction.
- Static isometric activities should be stopped such as prolong standing or carrying heavy weight.
Rhythmic movements should be encouraged such as swimming,massaging - Daily wearing of below-knee stockings
- Trauma and infection should be avoided.
- Complex decongestive therapy should be given.
It occurs in two phases, i.e. intensive therapy and maintenance therapy.
Lymphoedema Surgeries:
- Excision of lesion can be done by Charle’s or Homan’s operation.
- Physiological: Omentoplasty can be done.
- Combination ofExcision and physiological: Both excision and creation of communication between superfiial and deep lymphatics. Sistrunk and Thompson’s operation can be done.
- Bypass procedures can be done
- Limb reduction surgeries can be done.
Question.8. Write short note on clinical features of TB and its management, especially “DOTS regime”.
Answer. TB is a granulomatous disease caused by Mycobacterium tuberculosis.
TB Clinical Features
- Seen commonly in middle-aged and older individuals.
- Patient complains of episodes of fever with chills with evening rise of temperature. Patient becomes tired early.
- Presence of gradual loss of weight.
- Patient has persistent cough with or without hemoptysis.
- Swelling on neck is present which is fim and tender on palpation. When abscess is formed swelling perforates and pus drains out.
- Scrofula is the condition in which there is marked enlargement of cervical lymph nodes with caseation
- necrosis and frequent breakdown of gland.
- As skin is involved by tuberculosis, this is known as lupus vulgaris.
- Tubercular involvement of spine is called as Potts disease.
- When tuberculosis spreads through bloodstream it involves organs such as liver, kidney the disease is known as miliary tuberculosis.
TB Management—DotS Regimen
- Directly observed treatment strategy adopted by WHO is followed all over the World including India.
- Directly observed treatment means that an observer watches the patient swallowing their tablets.
- DOT ensures accountability of TB services and helps to prevent emergence of drug resistance.
TB Components of dotS
- Political and administrative commitment at all levels.
- Diagnosis through sputum microscopy
- Uninterrupted supply of short-course chemotherapy drugs.
- Direct observation of drug intake (DOTS)
- Systematic monitoring, evaluation, and supervision at all levels.
TB Dots Regimen
Note: Initial numeral before each regimen indicates the duration of therapy of that regimen. Numerals in subscript refer to thrice weekly schedule for the drugs.
Question.9. Give causes of cervical Lymphadenopathy and describe tubercular adenitis.
Answer.
Causes of Cervical Lymphadenopathy
Inflammation and infection:
1. Bacterial infections:
Specific bacterial infection
- Tuberculosis
- Syphilis.
Non-specific bacterial infection
- Pericoronitis
- Periodontal disease
- Peri-apical infections.
2. Viral infections:
- Infection mononucleosis
- AIDS
- Herpes simplex
- Cat scratch disease.
3. Fungal infections:
- Oral candidiasis
- Histoplasmosis.
4. Parasitic infections:
- Rickettsial Infection.
Allergic conditions:
- Serum sickness.
Primary neoplasms:
- Lymphoma.
Metastatic tumors:
- Oral squamous cell carcinoma
- Metastasis of carcinoma of breast.
Miscellaneous conditions:
- Leukemia
- Collagen diseases
- Sarcoidosis
- Non-tender lymphoid hyperplasia.
Question.10. Enumerate causes of cervical lymphadenopathy. Describe etiopathogenesis, clinical features and management of tubercular lymphadenopathy of neck.
Answer.
Etiopathogenesis
Mycobacterium tuberculosis is the bacteria which lead to tuberculosis. When the tubercle bacilli are introduced into the tissue.
- The initial response of neutrophils
- There is progressive infitration by macrophages
- Macrophages start phagocytosing the tubercle bacilli
- Activated CD4 + T cells develop
- In 2 to 3 days, the macrophages undergo structural changes and form epithelioid cells
- The epithelioid cells aggregated into tight clusters or granulomas
- Some macrophages form multinucleated giant cells
- Hard tubercles form by the mass of epithelioid cells and the giant cells in a zone of lymphocytes, plasma cells and firoblasts
- Center of the cellular mass undergoes caseous necrosis,characterized by cheesy appearance called as soft tubercle.
Question.11. Write short note on Lymphangitis.
Answer. It is an acute non-suppurative infection and spreading inflammation of lymphatics of skin and subcutaneous tissues due to beta-hemolytic streptococci, staphylococci,clostridial organisms.
- It is commonly associated with cellulitis.
- Erysipelas is a type of lymphangitis.
- In endemic areas, fiariasis is the most common cause (coastal India). It is caused by Wulchereria Bancroft.
Lymphangitis Clinical Features
- Streaky redness which is spreading is typical.
- On pressure, area blanches; on release redness reappears.
- Edema of the part, palpable tender regional lymph nodes are obvious.
- Fever, tachycardia, features of toxemia.
- Groin lymph nodes are enlarged and tender in lower limb lymphangitis.
- In upper limb, as lymphatics are mainly located on the dorsum of hand, edema and redness develops on the
- dorsum. Infection in thumb and index finger causes palpable tender axillary nodes; in litte and ring figer
- causes fist tender palpable epitrochlear nodes to appear; infection in middle figer causes fist deltopectoral nodes to enlarge.
- Toxemia, septicamia may occur.
- Rapidity may be more indiabetics and immunosuppressed.
- Chronic lymphangitis occurs due to repeated attacks of acute recurrent lymphangitis leading into acquired lymphoedema.
Lymphangitis Investigations
- Blood cell count
- Platelet count
- Renal and liver function tests
- Peripheral smear and blood culture
Lymphangitis Management
- Antibiotics such as penicillin, cloxacillin.
- Elevation, rest, glycerine magnesium sulpha dressing.
- Management of toxemia or septicemia with critical care.
Question.12. Enumerate diffrences between sinus of tuberculosis and actinomycosis.
Answer.
Question.13. Enumerate causes of cervical lymphadenopathy. How will you manage this?
Answer.
Cervical Lymphadenopathy Management
Acute Cervical Lymphadenopathy
- In a situation, where a self-limited infection is thought to be the etiology ofacute cervical lymphadenitis, it is reasonable to observe and provide reassurance.
- Unilateral lymphadenopathy that has a history of a rapid onset and overlying erythema of the skin and is accompanied by a fever suggests a bacterial infection. In this case, oral antibiotic therapy for 10–14 days and close follow-up is the appropriate management.
- An ultrasound may be indicated to evaluate for the presence and extent of suppuration.If confimed surgical drainage is required with the presence of a flctuant mass,suggesting an abscess.
- On follow-up of adenopathy, further evaluation should be considered, if there is not a decrease in size after 2 weeks.
- Laboratory evaluation may include the following: CBC with differential, ESR, titers for Ebstein-Barr virus/cytomegalovirus/toxoplasmosis/cat-scratch disease,antistreptolysin O or anti-DNAase serologic tests, PPD,and chest radiograph.
- Non-infectious causes of cervical lymphadenopathy include Kawasaki Disease, PFAPA (periodic fever, aphthous stomatitis, pharyngitis, and cervicaladenitis), and Sarcoidosis. Cervical lymphadenopathy is accompanied by a number of other signs and symptoms in each of these non-infectious disorders, and evaluation and management is individualized based on the disease.
Chronic Cervical lymphadenopathy
- Laboratory evaluation includes CBC, ESR, PPD, B henselae serology, and titers for Ebstein-Barr virus/cytomegalovirus/toxoplasma among other tests based on history and physical examination.
- Children who have chronic cervical lymphadenopathy often undergo extensive diagnostic evaluation before an etiology is determined.
- Special attntion should be given to the possibility of TB and HIV disease; the hematologic and serologic testing noted previously can be helpful.
- Urine antigen tests for Histoplasma capsulatum occasionally can be helpful.
- If there is an increase in lymph node size over 2 weeks,lack of decrease in size over 4–6 weeks, lack of regression to normal within 8–12 weeks, or the presence of persistent fever, weight loss, fatigue, night sweats, hard nodes, or fiation of nodes to surrounding tissues, a biopsy should be performed for further evaluation.
- Biopsy can be in the form of open biopsy or fie needle aspiration to further investigate for certain pathology,including infectious and non-infectious causes, specifically malignancy. Because lymphadenitis caused by nontuberculous Mycobacterium (NTM) evolves to draining skin fitulas associated with scarring, the safety of needle aspiration when this infection is suspected has been questioned.
- Needle aspiration may not lead to increased risk for this complication because the treatment of a node found to be infected with NTM is surgical excision-a cure for skin fistulas.
- NTM and Bartonella infection are diagnosed best using material obtained from a suppurative lymph node, which can be stained and cultured for acid-fast organisms and sent for polymerase chain reaction (PCR) examination to detect B henselae infection.
Importantly, PCR analysis for Bartonella can be performed on material that was obtained recently and preserved by freezing.
It is sensible to freeze extra material obtained by needle aspiration so PCR studies can be performed if bacterial studies are unexpectedly negative.
Question.14. Write briefly on Burkitt’s Tumor.
Or
Write short on Burkitt’s jaw tumor.
Answer. It is also known as African jaw lymphoma.
Burkitt’s Tumor Etiology
Epstein-Barr virus is considered to be the etiological factor.
Burkitt’s Tumor Types
- Endemic (African): Occurs commonly in jaw.
- Non-endemic (Sporadic): Occurs commonly in abdomen
- Aggressive lymphoma: In HIV patients.
Burkitt’s Tumor Clinical Features
- It is commonly seen in children during the age of 6–9 years.
- Males are commonly affcted as compared to females.
- Male to female ration is 2:1.
- Lesion is found most commonly in maxilla and spreads towards flor of the orbit.
- In African form jaw is more involved while in American form abdominal involvement is common.
- Lesion has very fast growth and it doubles in size within a day.
- Patient complaints swelling of jaw, abdomen and paraplegia.
- Peripheral lymphadenopathy is commonly seen.
- Renal involvement is present which can be bilateral.
- In females, ovaries are also affcted.
Burkitt’s Tumor Oral Manifestations
- Tumor is rapidly growing and involves maxillary, ethmoidal and sphenoidal sinus along with orbit.
- Presence of loosening and mobility of permanent teeth.
- Presence ofparesthesia ofinferior alveolar canals and other sensory facial nerves.
- Gingiva adjacent to affcted teeth become swollen, ulcer ated and necrotic.
- There can be presence of large amount of mass in the mouth on the surface of which present the rootless developing permanent teeth.
Burkitt’s Tumor Investigations
- Radiograph: It shows moth-eaten appearance with loss of lamina dura.
- Biopsy: Starry Sky appearance is characteristic for Burkitts lymphoma.
- USG: This done for abdomen so that kidneys should be evaluated.
- Blood urea and serum creatinine estimation is done.
Burkitt’s Tumor Treatment
- Radiotherapy.
- Chemotherapy, i.e. cyclophosphamide, methotrexate,orthomelphalan.
- Surgery is usually not indicated unless it is localized or in case of involvement of ovaries.
Question.15. Write briefly on Hodgkin’s Lymphoma.
Answer. Hodgkin’s lymphoma is a lymphoproliferative disorder which arises from lymph nodes and from lymphoid Components Of Various Organs.
Hodgkin’s Lymphoma Clinical Features
- The tumor is seen in young adults, i.e. during 20 to 30 years or in elderly people during 5th decade of life.
- Onset of the tumor is insidious with enlargement of one group of superfiial nodes.
- Associated lymph nodes are painless. There is presence of generalized weakness, cough, dyspnea and anorexia.
- Lymph nodes are discrete and rubbery in consistency with overlying skin is purely mobile.
- Pel-Ebstein fever is present, i.e. presence ofcyclic fever with generalized severe pruritus which is of unknown etiology.
- In oral cavity, the lesion appears as an ulcer or swelling.
- It can also be present as intrabony lesion which appears as hard swelling.
Ann Arbor Clinical Staging
Hodgkin’s Lymphoma Investigations
Blood test:
- Non-specifi anemia of chronic disease is common
- Lymphopenia is present.
- ESR is elevated.
Lymph node biopsy:
Show presence of Reed-Sternberg cells.
Hodgkin’s Lymphoma Imaging:
- Chest X-ray to look for mediastinal lymph nodes and pleural effusion
- CT is valuable in detecting intrathoracic and abdominal lymphadenopathy.
USG: To look for liver, spleen and abdominal lymph node.
Hodgkin’s Lymphoma Management
Stage I and II:
- Mainly radiotherapy, i.e. external high cobalt radiotherapy
- Above the diaphragm: Y fild therapy, covering cervical,axillary, mediastinal lymph nodes.
- Below the diaphragm: Mantle or inverted Y fild therapy covering para-aortic and iliac nodes.
- Chemotherapy is also given.
Stage III and IV:
- In this, mainly chemotherapy is given.
Regimens used are:
MoPP regimen
- Mechlorethamine: 6 mg/sqm on 1st and 8th day.
- Oncovine: 1.4 mg/sqm on 1st and 10th day.
- Procarbazine: 100 mg orally daily for 10 days.
- Prednisolone: 45 mg orally daily for 10 days.
- MOPP combination is given in 6 courses with no drugs given from 15th to 28th day.
ABVd Regimen
- Adriamycin: 30 mg/sqm
- Bleomycin: 10 mg/sqm
- Vinblastine: 6 mg/sqm
- Dacarbazine: 350 mg/sqm
The cycle is repeated on 20th day.
Splenectomy is done in many patients except with stage IV disease.
Question.16. Write short note on Lymphoma.
Answer. Lymphomas are the progressive neoplastic condition of lymphoreticular system which arises from stem cells.
Lymphoma is the third most common malignancy among the children.
Classifiation of Lymphoma
WHO modified REAL(Revised European American Lymphoma)
classifiation of lymphoma.
1. B-cell neoplasms:
- Precursor B cell neoplasm: ALL, LBL.
- Precursor B cell neoplasm: It includes all B-cell-related non-Hodgkin’s lymphomas.
2. T-Cell and putative NK cell neoplasms
- Precursor B-cell neoplasm: ALL, LBL T cell related.
- Precursor T-cell and NK cell neoplasm: It includes all T cell related non-hodgkin’s lymphomas.
3. Hodgkin’s lymphoma:
- Predominant Hodgkin’s lymphoma: Nodular lymphocyte type.
- Classical Hodgkin’s lymphoma:
- Nodular sclerosis
- Lymphocyte rich
- Mixed cellularity
- Lymphocyte depletion.
4. Precursor lymphoid neoplasms
5. Immunodeficiency-associated lymphoproliferative disorders.
ALL is Acute lymphoblastic leukemia.
LBL is Lymphoblastic lymphoma.
Lymphoma Etiology
- Genetic predisposition
- Sjogren’s syndrome
- HIV infection
- Virus etiology, i.e. Epstein-Barr virus infection
- Occupational causes: Hair dye workers, herbicide exposure
- Ionising radiation
- Celiac sprue—Intestinal T-cell lymphoma
- Bloom’s syndrome.
Types Of Lymphoma
- Hodgkin’s lymphoma
- Non-Hodgkin’s lymphoma
Question.17. Discuss differential diagnosis of cervical lymphadenopathy.
Answer. Following is the differential diagnosis of cervicofacial lymphadenopathy:
Infective Causes
- Acute lymphadenitis
- Chronic non-specifi lymphadenitis
- Tuberculous lymphadenitis
- Infectious mononucleosis
- Toxoplasmosis
- Cat scratch fever.
Neoplastic Causes
- Metastatic lymph node enlargement
- Lymphomas, i.e Hodgkin’s lymphoma, Non-Hodgkin’s lymphoma, Burkitts lymphoma
- Chronic lymphatic leukemia.
Other Causes
- Autoimmune diseases, i.e. systemic lupus erythematosus,rheumatoid arthritis.
- HIV infection, Immunosuppression.
Acute Suppurative Lymphadenitis
- It is a bacterial infection leading to acute inflmmation and suppuration of lymph nodes caused by group A streptococci or staphylococci.
- There is presence of tender, enlarged, fim or soft palpable neck lymph nodes.
Chronic Non-specific Lymphadenitis
- Infections such as chronic tonsillitis, recurrent dental
- infection can lead to chronic non-specifi lymphadenitis.
- There is presence of fim, non-tender, multiple, bilateral lymph node enlargement in neck.
- Tuberculous lymphadenitis
- It is caused by mycobacterium tuberculosis infection.
- Lymph nodes are mattd, enlarged with cold abscess or sinus formation.
Infectious Mononucleosis
- Caused by Epstein-barr virus.
- There is presence of generalized lymphadenopathy.
- Monospot test is positive.
Toxoplasmosis
- Caused by Toxoplasma gondii, protozoa through meat.
- Cervical lymphadenopathy is most common.
- Diagnosed by Sabin Feldman dye test.
Cat Scratch disease
- Caused by Bartonella henselae.
- Lymphadenopathy is present.
- Diagnosed by lymph node biopsy with Warthin-Starry staining.
Lymphomas
- In Hodgkin’s lymphoma, there is painless progressive enlargement of lymph nodes.
Lymph nodes are smooth,firm, non-tender. In this cervical lymph nodes, i.e. lower deep cervical group in posterior triangle are commonly enlarged.
In this type, peripheral lymph node involvement is not common. - In non-Hodgkin’s lymphoma any group of lymph node is involved. In this type, peripheral lymph node involvement is common.
Question.18. Write briefl on chemotherapy of tuberculosis.
Answer. Category-wise Alternative Treatment Regimens for Tuberculosis (WHO-1997)
Explanation Of Standard Code
- Each antitubercular drug has standard abbreviation, i.e.
- Isoniazid (H)
- Rifampicin (R)
- Pyrazinamide (Z)
- Ethambutol (E)
- Streptomycin (S).
- Numerical before a phase is the duration of that phase in months.
- Numerical in subscript is the number of doses of that drug per week. If there is no subscript numerical, then the drug is given daily.
Question.19. Name etiological agent, pathognomic diagnostic feature, and treatment (only modalities) of matted lymph nodes in neck.
Answer.
Etiological Agent
Since mattd lymph nodes in neck are seen in tuberculosis, the etiological agent is Mycobacterium tuberculosis.
Pathognomic diagnostic Feature
Matting of lymph nodes in neck is itself a pathognomic diagnostic feature of tuberculosis.
Mattng is due to involvement of capsule. Nodes are firm and non-tender.
Mattng is due to involvement of capsule. Nodes are firm and non-tender.
Treatment (Only Modality)
Anti-tubercular treatment should be given to the patient.
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