When the scan suggests cancer in the lymph nodes in the middle of the chest, EBUS is usually the first test, because it is the least invasive route to a diagnosis or a nodal stage. When needle sampling has not answered the question, removing the lymph node can provide the tissue needed to settle it. A cervical mediastinoscopy takes whole nodes from the centre of the chest through a small incision at the base of the neck, under general anaesthetic, as a day case. It is used when an endoscopic result is negative, inadequate or discordant; when the diagnosis depends on the structure of the node as well as its cells; when the tissue must carry a full molecular panel; and when the nodal stage itself will decide the treatment. Dr Okiror performs mediastinoscopy at London Bridge Hospital and The Lister Hospital Chelsea, and in his NHS practice at Guy’s and St Thomas’. Self-referrals welcome, and referrals accepted from oncology, haematology and respiratory medicine.
Last reviewed: October 2026 · Dr Lawrence Okiror FRCS(CTh) FRCSEd(CTh) · GMC 6150382
Whole Nodes
Intact lymph nodes are removed, with their architecture preserved, from stations 2R, 2L, 4R, 4L and 7.
Day Case
Admitted in the morning, home the same day in the great majority of patients. General anaesthetic.
28 Cases, Six Years
Across six audited years of SCTS returns, and roughly 26% of all mediastinoscopies performed in his department.
Endobronchial ultrasound with transbronchial needle aspiration is the first-line test for sampling lymph nodes in the centre of the chest. A camera with an ultrasound probe on its tip is passed into the airway, the nodes are seen through the airway wall, and a needle is passed into them under direct ultrasound vision. It reaches the paratracheal and subcarinal stations reliably, it is performed under sedation without an incision, and its diagnostic yield for common pathology is high. For staging lung cancer and confirming metastatic disease in the glands, it answers the question in most patients. It has replaced mediastinoscopy as the initial procedure.
Its limits are specific:
Reach
The scope works from inside the airway, so a node must sit against it to be sampled. Lesions in the prevascular compartment, in front of the great vessels, lie in a different anatomical plane.
Volume
A needle recovers cells and small cores. That is sufficient for most diagnoses and for most molecular work, and occasionally it is not sufficient for everything a modern panel asks of one specimen.
Architecture
Some diagnoses depend on how cells are arranged within the node rather than on the cells alone. Lymphoma is the clearest example, and granulomatous disease behaves similarly.
Tolerance
EBUS is usually done under sedation. Severe cough, airway compromise or anxiety mean that some patients cannot complete it, and a previous abandoned attempt is a common referral.
A mediastinoscopy addresses each of these for one physical reason: it removes whole lymph nodes instead of sampling them through a needle. It provides an intact node, including its architecture, when that is what the diagnosis depends on.
EBUS techniques continue to develop. EBUS-guided transbronchial mediastinal cryobiopsy passes a fine cryoprobe into the node through the airway, freezes a core of tissue and retrieves it. The specimen is substantially larger than a needle aspirate and considerably better preserved, which addresses two of the four limitations set out above.
The published results are strong, particularly in exactly the disease where surgical biopsy has traditionally been argued for. A prospective multicentre study in suspected lymphoproliferative disorders found a diagnostic yield of 80% for cryobiopsy against 52% for needle aspiration, rising to 85% against 41% in confirmed cases, with 80% of non-diagnostic aspirates subsequently diagnostic on cryobiopsy. A systematic review reported cryobiopsy diagnostic in 87% of lymphomas against 12% for needle aspiration, and able to characterise every lymphoma subtype. A randomised trial in non-metastatic lymphadenopathy found 97.1% against 79.9%.
A modified Delphi consensus statement published in CHEST in 2026, involving 32 physicians across four survey rounds, provides the first formal expert guidance for the use of transbronchial cryobiopsy outside interstitial lung disease, including convex-probe EBUS-guided cryobiopsy and specimen handling. It was produced because practice had spread faster than standardisation; it reached consensus on some questions and not on others.
Cryobiopsy narrows one of the traditional reasons for proceeding to mediastinoscopy. It does not close the indications where definitive surgical staging is what the treatment decision requires, where an intact node is specifically needed, or where the endoscopic route has already been attempted without an answer. It is also concentrated in centres with established EBUS and cryobiopsy expertise, so the alternative available to a particular patient depends on where they are being investigated.
Five situations, in the order they arise in practice. They overlap. In each, a needle result has not resolved the clinical question.
One
Negative, inadequate, or discordant with the clinical picture. A negative needle result in a patient whose imaging and history point firmly at nodal disease leaves the question unanswered. Where the pre-test probability is high and the treatment decision depends on the answer, sampling the nodes surgically is the proportionate next step.
Two
Lymphoma above all, and selected uncommon tumours. Where the pattern within the node carries the diagnosis, the sampling method is chosen with the haematopathologist. An intact node is one way of providing that; cryobiopsy is increasingly another, and which is appropriate depends on the node, the differential, and what is available.
Three
Confirmation of staging before neoadjuvant treatment is a request Dr Okiror receives from the multidisciplinary team and has acted on. The modern pathway turns on the nodal stage: whether systemic treatment comes first, whether surgery is an option, and in what order. Where the endoscopic answer is equivocal and the decision rests on it, the stage should be established definitively. A lymph node that has been seen on a scan and never sampled is a reason to ask before stage 3 is accepted. If you have been told an operation is not possible because of the lymph nodes, see told surgery is not an option: the reasons given, and which of them can change.
Four
A failed or intolerable EBUS, an anatomical limitation, or a node that the endoscopic route cannot reach. Mediastinoscopy is performed under full general anaesthetic, so the tolerance problem does not arise. Where cryobiopsy would be the natural alternative but is not available locally, the practical choice is between repeating a needle and taking the node.
Five
Selected diagnostic problems where a whole node is specifically required. Suspected recurrence in a previously treated field, a node that has been sampled twice without a clear answer, an unusual differential where the pathologist has asked for more material, disease after previous chemotherapy or radiotherapy (see surgery after radiotherapy) where the tissue is necrotic and a needle keeps returning debris. In each case the question is what the laboratory will need to give a definite answer, and the least invasive way of providing it.
Lymphoma is one of the situations in which preserving tissue architecture can be decisive. It commonly presents with B symptoms, drenching night sweats and weight loss, before any node is palpable. The diagnosis frequently depends on the abnormal cells and on how they are arranged within the node: whether the pattern is follicular or diffuse, how far the normal structure has been effaced, the relationship of the infiltrate to the capsule and the sinuses. Subtyping under the current WHO classification then requires immunophenotyping, flow cytometry and molecular studies, each of which consumes material. Lymphoma is also the commonest non-surgical cause of chylothorax; when a chylous effusion accompanies mediastinal lymphadenopathy, the node biopsy establishes the diagnosis and the effusion is managed on its own pathway.
The biopsy method should therefore be chosen in discussion with the haematologist and the haematopathologist. Some subtypes are reliably diagnosed on small samples; others are not. An inadequate specimen delays the diagnosis and risks an incomplete or incorrect one; treatment in lymphoma is subtype-specific.
Excisional biopsy remains an important approach where an intact node is required, and where the abnormal nodes are confined to the mediastinum a cervical mediastinoscopy is the route that reaches them. At the same time, EBUS-guided cryobiopsy is increasingly able to provide larger and more architectural samples from selected mediastinal nodes, and where it is available it is a reasonable step before surgery.
What should not happen is a succession of small-volume samples taken in sequence, each inadequate for the same reason, while the diagnosis waits. If the first sample was reported as insufficient for lymphoma assessment, the next attempt should be chosen to answer that specific problem.
A diagnosis of adenocarcinoma is now the start of the tissue requirement. The same specimen may need to support immunohistochemistry to confirm the subtype, PD-L1 scoring, and broad molecular profiling across a panel that now routinely includes EGFR, ALK, ROS1, BRAF, KRAS, MET, RET and NTRK, with next-generation sequencing requiring a minimum tumour cell content and DNA yield. Occasionally the tumour volume recovered will not stretch to all of it.
EBUS-TBNA supports molecular testing in most patients. The situation described here is narrower: the laboratory has reported insufficient tumour or insufficient material, and the treatment decision is waiting on a result that cannot be produced from what was sent.
In that position, obtaining a larger specimen may be necessary instead of repeating the same small-volume sampling. Oncology colleagues ask Dr Okiror to perform mediastinoscopy for this reason: the demands on the tissue have grown since the first sample was taken.
The wider sequence of investigations before treatment, and where nodal sampling sits within it, is set out on the lung cancer tests and staging page.
The operation is performed under general anaesthetic with the neck slightly extended. A transverse incision of about 3 cm is made at the base of the neck, sitting in a natural skin crease just above the sternal notch. The strap muscles are separated in the midline and the plane immediately in front of the trachea is opened, first with a finger and then under direct vision, so that the mediastinoscope passes down alongside the windpipe into the centre of the chest.
From that position the nodal stations used for staging and for diagnosis are within reach: 2R and 2L in the upper paratracheal region, 4R and 4L lower paratracheal, and station 7 beneath the carina where the trachea divides. Nodes are dissected free and removed whole. Where a lesion is being sampled for diagnosis rather than staged, tissue is taken generously, because the commonest reason for a repeat procedure is a specimen that was too small for what the laboratory was later asked to do with it.
Selected specimens may undergo intraoperative assessment where an immediate result would alter the procedure being performed. That answers a specific question on the day; it is not the final diagnosis. Definitive histopathology, and any required immunohistochemistry, flow cytometry or molecular testing, follow afterwards.
The wound is closed in layers with an absorbable suture placed beneath the skin, so there are no stitches to remove. A drain is not usually required.
Other surgical routes
Cervical mediastinoscopy reaches the paratracheal and subcarinal stations. It does not reach everything. Lesions in the prevascular compartment are approached by anterior mediastinotomy through a small incision beside the sternum, and lesions in the aortopulmonary window or the paravertebral compartment by a VATS or robotic approach. Which route applies is an anatomical decision made on the cross-sectional imaging; the full range is described on the mediastinal surgery page.
Dr Okiror performs mediastinoscopy as a day case. You are admitted in the morning, having eaten nothing from midnight, and seen by the surgeon and the anaesthetist before going to theatre. The operation itself takes under an hour in most cases. You wake in recovery, spend a few hours on the ward, eat and drink, and go home the same day.
You will need a responsible adult to collect you and stay with you overnight, as after any general anaesthetic, and you should not drive, operate machinery or sign anything legally binding for 24 hours. Most people take a few days off work. Discomfort is usually a sore throat from the breathing tube and a sore neck from the dissection, controlled with simple analgesia.
Who stays overnight instead. Patients with significant cardiac or respiratory comorbidity, patients on anticoagulation that requires monitored reversal and restart, those who live a long way from the hospital or have nobody at home, and the occasional patient whose operation proved more difficult than the imaging suggested. That possibility is discussed before the day.
Day-case status has a particular value here. This is a diagnostic operation performed on someone who does not yet know what they have, frequently while a treatment decision waits. A procedure that costs one day rather than an inpatient admission is easier to accept and quicker to arrange.
Mediastinoscopy is a well-established operation with a low complication rate in experienced hands. It is still an operation, and consent covers the risks set out below.
Common and self-limiting: sore throat, a sore or stiff neck for a few days, bruising around the incision, and temporary discomfort on swallowing.
Uncommon: hoarseness, where the nerve supplying the voice box is stretched or irritated during dissection, more relevant on the left, where that nerve loops beneath the aortic arch close to the operative field. It is usually temporary. Wound infection is unusual in a clean neck incision.
Rare but serious: bleeding from the large vessels lying immediately alongside the dissection, injury to the trachea or oesophagus, and pneumothorax. Any of these would convert a short day-case operation into a larger one, potentially requiring sternotomy. They are rare, and they are the reason this operation should be done by surgeons who perform it regularly.
There is also a diagnostic limitation: a mediastinoscopy samples the stations it can reach. A negative result is strong evidence about those stations and says nothing about nodes elsewhere in the chest. Where the imaging points to a compartment outside its reach, a different route is chosen from the start.
Definitive histopathology usually takes several days. Where immunohistochemistry, flow cytometry or molecular profiling are required, the complete result takes longer, commonly one to three weeks depending on the panel requested. That wait should be anticipated. The result is discussed at the multidisciplinary team meeting and then gone through with you directly.
Where the answer changes the treatment plan, the referring oncologist, haematologist or physician receives it at the same time, so that the next step is arranged without a further round of appointments.
In this practice
Across six audited years of SCTS returns, Dr Okiror performed 28 cervical mediastinoscopies, and carried out approximately 26% of all mediastinoscopies performed in his department over the five years for which departmental and personal returns reconcile. Mediastinoscopy has become less common nationally as endoscopic sampling has improved, so regular experience of it is a reasonable question to ask of any surgeon.
How the diagnostic routes fit together
There are three routes, each with a different target. ION navigational bronchoscopy obtains tissue from a lesion out in the lung itself, without an incision. EBUS samples and stages the lymph nodes in the centre of the chest through the airway wall. A mediastinoscopy provides surgical nodal tissue when the endoscopic route has not answered the question. They are complementary, and the right one depends on where the tissue has to come from and what the laboratory will be asked to do with it.
A guide price for a cervical mediastinoscopy at London Bridge Hospital is £8,000–£12,000, covering hospital, surgeon and anaesthetist fees for an uncomplicated stay. Hospital charges are the largest part of the total. The hospital issues a written fixed quote after consultation and before treatment, and that quote is the figure that applies. All guide prices and how fees work →
Dr Okiror is recognised by AXA Health, Bupa, Aviva, Vitality, WPA and Cigna, and by most other UK and international insurers. If you have private medical insurance, Dr Okiror and the hospital bill your insurer directly, and insurers usually settle the hospital, surgeon and anaesthetist fees in full, less any excess written into your policy. Please confirm with your insurer that your policy covers treatment at London Bridge Hospital or The Lister before your first appointment. Self-paying patients are equally welcome.
How quickly treatment happens. Patients who already have their tests can be booked for surgery within days of their consultation.
Questions from patients whose EBUS has not given an answer, and from referrers deciding which sampling route will provide the tissue the diagnosis needs.
Book a Consultation →Or call Jo Mitchelson:
020 7952 2882
Appointments within 2–3 days. Self-referrals welcome. Referrals accepted from oncology, haematology and respiratory medicine. Day-case surgery at London Bridge Hospital and The Lister Hospital Chelsea.
Jo Mitchelson, PA · 020 7952 2882 · pa@lungsurgeon.co.uk
St Thomas’ Hospital #1 UK · Guy’s Hospital #2 UK · London Bridge Hospital #10 UK · Newsweek World’s Best Hospitals 2026
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