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e144

Abstracts of the 22

nd

National Congress of Digestive Diseases / Digestive and Liver Disease 48S2 (2016) e67–e231

inflammation. The positive effect of the eradicant Hp treatment may

also produce a reduction in serum levels of PGII.

The aim of the study was to assess the combined role of PGII and

anti IgG Hp antibodies (Hp abs) serum levels in the diagnosis of Hp-

related gastritis and in the follow-up after eradication.

Material and methods:

A total of 657 dyspeptic patients (M=219,

F=438, mean age=44.4±14.0 ys, range=18-86 ys) were evaluated.

PGII concentrations and Hp abs were determined via an ELISA test

(GastroPanel, Biohit Oyi, Helsinki, Finland) in fasting serum samples.

Patients affected by chronic atrophic gastritis were excluded from

the study. Patients in proton pump inhibitors (PPI) were included.

Results:

170 patients of 657 (25.9%) were Hp positive and 487 Hp

negative (74.1%). The table shows the result of age, PGII and Hp abs

in the four groups of patients.

Table 1

No PPI treatment

With PPI treatment

H pylori status

Age

PGII

IgG Hp Age

PGII

IgG Hp

Negative

38.4±10.8 5.8±2.5 6.5±10.4 42.4±13.4 8.4±4.2 7.1±8.7

Positive

39.1±10.8 12.9±6.7 90.3±24.5 43.7±14.0 17.3±12.1 83.5±30.8

Eradicated

45.6±13.3 5.8±1.6 30.7±31.3 55.1±13.1 8.1±4.1 24.0±23.2

(Hp-ve)

Non eradicated 54.2±13.2 12.4±3.8 86.5±30.7 52.9±13.5 19.9±14.4 81.8±36.5

(Hp+ve)

Conclusions:

The combined use of serum PGII (>10 ug/L) and Hp

abs (>=30 EIU) levels most accurately defines a picture of Hp-related

gastritis; the reduction of PGII concentrations under 10 ug/L as well

as Hp abs <30 EIU could be may be an aid in evaluating the efficacy

of eradication therapy.

P.04.4

THE SHOWER IS NOT WARM ENOUGH!

Padula D.*, Lenti M.V., De Quarti A., Miceli E., Corazza G.R.

Clinica Medica I IRCCS Fondazione Policlinico San Matteo, Pavia, Italy

Background and aim:

A 30 years old Caucasian female, presented

with a 7 years history of nausea and non bloody hyperemesis 5 times

daily. She had multiple hospitalizations and emergency accesses

during the past years for intermittent abdominal pain, nausea and

vomiting and referred important weight loss (of about 15 Kg in the

last 3 years).

Material and methods:

An extensive medical workup had

demonstrated negative, including upper and lower endoscopy,

magnetic resonance enterography (jejunal thickening), PET scan,

push endoscopy. Moreover in the last three years she reported a

progressive increase of the systolic pressure, mean values over 160

mmHg, an ultrasound study of the renal arteries showed no arterial

obstruction.

Results:

At the admission to our Clinic the physical examination

showed increased levels of blood pressure (160/90mmHg), routinary

laboratory tests were unremarkable. She reported smoking one

cigarette daily and occasional alcohol use in social settings. No

family history of hypertension or gastrointestinal disorders was

declared.

During the first days of hospitalization she actually presented

an intractable vomit of whitish watery secretions associated to

abdominal pain and continuous nausea, antiemetics, including

metoclopramide and onsansetron, were not effective in relieving

the symptoms, she reported that the only strategy that could help

relieve her nausea was hot water, complaining that the hospital

showers were not warm enough. Her workups included: upper GI

with barium, gastric emptying studies (14C-octanoic acid gastric

emptying breath test), US abdomen, abdominal computerized

tomography; none of these investigations revealed pathology. After

a few days, the symptoms underwent to spontaneous relapse, in

those days she returned to normal bath habits.

Conclusions:

In order to exclude toxic ingestion other tests were

performed and showed the presence of cannabis in urine and blood

stools. She admitted smoking cannabis from at least 8 years.

The diagnosis of “cannabinoid hyperemesis syndrome” was made,

we recommend to quit smoking. On follow-up 6 months later,

she had remained free of cannabis use and she had no symptoms

of nausea, vomiting or compulsive bathing, moreover the blood

pressure levels returned normal.

P.04.5

PROGNOSIS OF GASTRIC GISTS BASED ON TUMOR SIZE

Togliani T.*, Mantovani N., Vitetta E., Savioli A., Troiano L., Pilati S.

S.S.D. di Endoscopia Digestiva, Azienda Ospedaliera Carlo Poma,

Mantova, Italy

Background and aim:

Gastric GISTs range from small benign lesions

to large metastatic tumors; EUS provides diagnostic and prognostic

information that help deciding between follow up or surgery. The

aim of this study was to establish the prognostic value of the size of

gastric GISTs.

Material and methods:

We retrospectively studied patients with

an EUS diagnosis of gastric GIST without metastases; we divided

them according to the initial size of the tumor: Group A (≤2 cm),

Group B (>2 cm). The clinical onset and the EUS characteristics were

recorded. For the prognostic evaluation one among these follow up

data was required: an EUS control after ≥6 months, the histologic

diagnosis in operated patients, or the documentation of a GIST-

related death.

Results:

Fifty-two patients were included. Group A was composed

of 24 patients. The onset was dyspepsia in 21 cases, anemia in 2,

a CT suspect of GIST in 1. EUS worrisome criteria (inhomogenicity,

irregular borders, enlarged lymph nodes, ulceration) were present

in 5 cases. After a mean of 45 months EUS controls showed no

changes in 19 patients and a little worsening (a mild enlargement

or the appearance of a second <1 cm GIST) in 4; 1 patient died after

GIST bleeding. No patients were operated. Group B was composed of

28 patients. The onset was dyspepsia in 11 cases, anemia in 1, upper

GI bleeding in 6, a CT suspect of GIST in 10. EUS worrisome criteria

other than size were present in 25 patients. In the 22 operated

patients histology revealed 4 GISTs with high mitotic rate, 13 GISTs

with low mitotic rate, 5 other benign tumors. Because of their poor

general condition, 6 patients were not operated: 3 showed no EUS

worsening during follow up, 3 died for GIST progression.

Conclusions:

In Group A and Group B an alarming onset was present

in 13% and 61%, other initial EUS worrisome criteria were visible in

21% and 89%, signs of a bad evolution (an EUS worsening during

follow up, a high risk histology after resection or a tumor-related

death) were seen in 21% and 32%, respectively. GISTs belonging to

Group A and B probably represent the same disease diagnosed in

different moments: ≤2 cm GISTs were accidentally found in younger

patients (mean age 59 years) while >2 cm GISTs were seen in older

subjects (mean age 69 years) in whom tumors had more time to

grow, becoming symptomatic. Thus, as a minority of small GISTs

showed a slow and late progression, these patients can initially

avoid surgery but a long EUS follow up is mandatory (e.g. every 1-2

years for at least 10 years).