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Major
Diagnostic Advance: Bilateral Inferior
Petrosal Sinus Sampling in Cushing's Syndrome
by Beverly M.K. Biller, M.D.
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Diagnostic Problem
Cushing's syndrome, with its high morbidity
and mortality, requires a diagnostic workup which includes verifying
the patient's cortisol excess, then documenting the site of hormone
overproduction. ACTH-dependent causes include pituitary tumors (Cushings
disease) and ectopic ACTH-secreting (or rarely CRH-secreting) tumors,
while ACTH-independcnt Cushing's is due to a primary adrenal lesion(Figure
1).
Figure 1 From Schteingart DE: Cushing's syndrome in EndocrinoIogy
and Metabolisrn Clinics of North America Barkan AL (ed), Vol.
18, No. 2, June 1989; with permission.
The most common cause of Cushing's syndrome is Cushing's disease,
but 15% of all cases are due to ectopic productioti of ACTH (and
rarely GRH). The classical ectopic Cushing's syndrome cases, usually
due to small cell carcinonia of the lung, are easy to distinguish
from pituitary Cushing's because of markedly elevated ACTH and failure
to suppress urine cortisol and its metabolites with high dose dexarnethasone.
However, many patients are being recognized as having benign occult
ectopic Cushing's, most co~nonly due to carcinoid tumors, with bronchial
carcinoid being the most frequent subtype. A recent series has shown
that in most patients with bronchial carcinoid, the clinical features
are typical of pituitary Cushing's, the tumor is occult in about
two-thirds of the patients, and the clinical course is often prolonged,
with a delay in diagnosis of up to 18 years. Most patients with
this disorder have normal to mildly elevated ACTH levels, and more
than half have dexamethasone sup-pressability, traditionally believed
to be diagnostic of pituitary Gush-mg's. Therefore, bronchial car-cinoid
may produce a clinical and biochemical pattern identical to that
seen in pituitary Cushing's. This presents a serious diagnosnc dilemma
in determining whether the patient shoutd have pituitary or chest
surgery.
Figure 2 Reprinted, by permission of The New England Journal of
Medicine Vol. 312 p. 101, 1985.
BIPSS Technique
The most important recent advance in the
diagnostic evaluation of patients with Cushing's syndrome has been
the use of bilateral inferior petrosal sinus sampling (BIPSS) for
AGTH The infrrior petrosal sinuses receive drainage from the pituitary
gland without 1rn'cture of blood from other sources. Therefore, if
the patient has pitui-tary Cushing's, the AGTH levels in the IPS are
high compared to an AGTH drawn in the periphery. in contrast, in ectopic
Cushing's, the AGTH in the IPS and the periphery should be equivalent
because the tumor is located elsewhere. The test is usually performed
by vascu-lar radiologists on an outpatient basis. With local anesthesia,
fenioral catheters are advanced bilaterally up to the inferior petrosal
sinuses (Figure 2). After confirmation of catheter location by fluoroscopy,
several ACTH samples are drawn simultaneously from the right and left
at the same time that a peripheral level is being drawn from an arm
vein. GRH can also be injected to provoke ACTH release. Samples are
then assayed for ACTH, and the pituitary-to-peripheral ratios are
calculated.
Bilateral Inferior Petrosal Sinus
Catheterization
| Patient |
ACTH in pg/ml |
Ratios |
| ID |
Right IPS |
Left IPS |
Peripheral |
Pit/Periph |
R/L |
| 1. |
288 |
62 |
44 |
6.5 |
4.6 |
| 2. |
144 |
62 |
55 |
6.5 |
2.3 |
| 3. |
514 |
68 |
58 |
8.9 |
7.6 |
| 4. |
544 |
73 |
68 |
8.0 |
7.3 |
| 5. |
913 |
88 |
60 |
15.2 |
10.4 |
Localization
If the pituitary-to-peripheral ratio is
greater than 2 (greater than 3 if GRH was given) the patient has Cushing's
disease, with a sensitivity and specificity of 100% if CR14 is used.
If the pituitary-to-peripheral ratio is less than 1.5 to I (less than
3 if GRH was given) the patient has ectopic Cushing's. This test,
therefore, allows certainty as to the location of Cushing's syndrome,
thereby directing the correct surgical approach
Lateralization
A feature of pituitary anatomy is that
each half of the pituitary drains into the ipsilateral IPS, often
making it possible to localize the tumor to the pituitary gland and
to determine which side it is located on (to lateralize it). In 20%
of patients the neurosurgeon is not able to locate the pituitary tumor
intraoperatively. Now, if sampling data suggest lateralization, the
neurosurgeon can explore that side. The IPSS is correct in predicting
tumor location in approximately two-thirds of cases. However, because
it is not always correct, it is important that the neurosurgeon explore
the other side if no tumor is found on the predicted side. Shown above
are results of BPSS in an individual patient. There were five ACTH
samples drawn q 5 minutes. As can be seen, all of the samples show
a pituitary-to-peripheral ratio greater than 2, confirming a pituitary
source of the Cushing's. In addition, all the samples show a right-to-left
gradient of greater than 1.4 to 1, documenting that the tumor is likely
to be on the right side. This patient did have a right-side pituitary
microadenoma and was cured following pituitary surgery at the Massachusetts
General Hospital.
Some rare difficulties in ability
to localize and lateralize
| Failure to Localize |
Failure to Lateralize
|
|
| 1. Inability to Catheterrize |
1. Incorrect Catheter Placement |
| 2. Incorrect Catheter Placement |
2. Sample Withdrawl was too Rapid |
| 3. Anomalous Venous Drainage |
3. Midline Microadenoma |
4. Hypercortisolemia Not Present
due to
medical therapy, s/p adrenalectomy, periodic hormonogeneis |
4. Prior Transsphenoidal Surgery |
| 5. Ectopic Tumor Secreting CRH |
5. Ectopic Tumor Secreting CRH |
Complications
Complications are infrequent, with the
most common being a hematoma at the groin site and transient ear pain.
The NIH recently published data on four patients who had neurologic
complications following the BIPSS in a total series of 500 patients.
In all four patients, a catheter design developed at the NIH was used
and all four patients experienced neurologic symptoms duriug the procedure.
In the two cases where the patients were reassured and the procedure
continued, permanent neurologic damage ensued. In the two cases where
the procedure was stopped immediately after development of symptoms,
all neurologic problems resolved within 48 hours.
Summary
In summary, BIPSS offers a major advance
in establishing the correct location of hormone excess in patients
with Cushing's syndrome. In many centers, it is performed in all patients
who do not have a definite macroadenonia seen on MRI. This test should
eliminate completely those "surgical failures" which were
actually diagnostic failures, and thereby provide better treatment
for patients with Cushing's syndrome.
References
- Leinung MC, et al. Diagnosis of
corticotropin-producing bronchial carcinoid tumor causing Cushing's
disease. Mayo Clinic Proc. 1990;65:1314.
- Oldfleld EL, et al. Petrosal sinus
sampling with and without corticotropin-releasing hormone in the
differential diagnosis of Cushing's syndrome. N Eng J Med. 1991;325.897.
- Miller DL. Neurologic complications
of petrosal sinus sampling. Radiology. 1992,185:143.
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