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Surviving Against All Odds: Analysis of
6 Case Studies of Patients With Cancer
Who Followed the Gerson Therapy
A. Molassiotis, RN, PhD, and P. Peat, RGN, DiplPallCare
Case 5
This case is a 68-year-old man (at the time of death;
born in 1935) diagnosed with (inoperable) cholangiocarcinoma.
Diagnosis was established by visual analysis of endoscopic retrograde cholangiopancreatography
and supported by CT scanning. The histology
report of pancreatic tissue suggests atrophy and
inflammation, with no malignant cells in the biopsy
specimen.
He was diagnosed in May 1997 at the age of
62 years following investigations for obstructive jaundice.
The tumor was felt to be resectable, and the plan
was to proceed with surgery. Upon laparotomy on
June 9, 1997, the tumor was found to be unresectable
because of extensive involvement of the portal vein,
and biliary bypass was performed.
Chemotherapy was
offered as a treatment option, but the patient
declined and started on the Gerson regimen in
August 1997. A magnetic resonance imaging (MRI)
scan on July 31, 1998, reported a 4-cm stricture in the
common bile duct, with an irregular soft tissue mass
visible at the liver hilum.
The hepatic artery was seen
to be surrounded by tumor in the superior portion of
the pancreatic head. An MRI scan on October 5,
1999, suggested that the tumor was progressing but at
a very slow pace. The patient was suffering no symptoms
at the time.
A review on November 14, 2000,
reported a 7 × 7 cm irregular mass in the portal vein,
CA 19-9 of 70, no ascites, and no metastatic liver disease,
remaining asymptomatic. A review on November
8, 2001, reported a CA 19-9 of 204, and physical examination
revealed an unremarkable abdomen.
A review
on February 5, 2002, reported evidence of activity in
the tumor; magnetic resonance cholangiopancreatography
showed a large tumor mass extending up
the hilum, around the duodenum, and infiltrating
the retroperitoneum.
An MRI scan report on February
13, 2003, showed a tumor at the head of the pancreas,
now 8 cm, invading the left lobe of the liver. A small
amount of ascites was present.
The patient’s disease
then progressed steadily until his death from cholangiocarcinoma
in April 2003.
Integr Cancer Ther 2007; 6; 80
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