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S102

Poster presentations / European Geriatric Medicine 6S1 (2015) S32

S156

P-263

Cryptogenic organizing pneumonia: a rare syndrome even

in the elderly. Case report

S. Zannoni

1

, C. Lorenzi

2

, M. Paoli

2

, F. Orso

3

, M. Torrini

4

,

M. Rafanelli

5

, G. Toffanello

5

, A. Giordano

6

, F.C. Gori Sacco

4

,

N. Marchionni

3

, A. Ungar

7

1

AOU Careggi Universit`a degli studi Firenze, Firenze, Italy;

2

AOU Careggi Universit`a degli studi Firenze, Florence, Italy;

3

Geriatric

Cardiology and Medicine, Careggi Univesrity Hospital, Florence,

Florence, Italy;

4

Geriatric Cardiology and Medicine, Careggi Univesrity

Hospital, Florence, Italy;

5

Geriatric Cardiology and Medicine,

University of Florence and AOU Careggi, Florence, Italy;

6

Italy;

7

Azienda Ospedaliero Universitaria Careggi, Florence, Italy

Patient:

Woman 88 years. Hospitalizazion for persistent low-grade

fever and dyspnea with worsening of respiratory exchanges. Chest

CT with contrast showed the involvement of the upper and lower

interstitial lung lobes with bilateral pleural effusions.

Empirical antibiotic therapy for nosocomial pneumonia was started.

For the persistence of symptoms was placed on suspicion of

cryptogenic Organizing Pneumonia (COP).

It was undertaken therapy with high dose of corticosteroids

with rapid clinical and radiological improvement. A chest

CT pre-discharge featured complete resolution of pulmonary

consolidations. The patient is currently in good condition and

assumes prednisone 12.5mg / day.

Results:

COP appears most frequently in the fifth-sixth decade of

life and affects men and women equally. It begins with cough,

dyspnea, fever, malaise and weight loss. Breathing pattern directs

toward the diagnosis of pneumonia, confirmed by radiological

evidence: typical is the presence of opacity, circumscribed or

diffuse, or consolidations with ground-glass appearance, often

migrants, with bilateral and peripheral distribution.

The most effective therapy is long-term administration of

corticosteroids at high doses that are gradually climbing in 6–12

months.

The complete resolution of the clinical picture and the

normalization of the radiological image usually occurs in 2/3

of patients. In patients who don’t respond to steroid therapy is

necessary to reconsider the initial diagnosis of COP.

Conclusion:

This case report may be useful for Geriatricians, since

our patient developed the disease beyond 80 years. The clinical

course may be similar to more frequent polymyalgia rheumatic in

the elderly, but these are just hypotheses.

P-264

Autoimmune hemolytic anemia in the elderly over 75 years:

report of a rare retrospective study

A.-A. Zulfiqar

1

, R. Mahdi

1

, J.-L. Pennaforte

1

, J.-L. Novella

2

,

E. Andres

3

1

CHU Reims, Reims, France;

2

France;

3

CHRU Strasbourg, Strasbourg,

France

Objectives:

Autoimmune hemolytic anemia is a rare disease in the

elderly.

Methods:

Retrospective study over a period of 5 years, focused on

two Internal Medicine Service (Reims and Strasbourg).

Results:

7 patients were enrolled, including two men. The average

age was 85.4 years. All had clinical signs of anemia (dyspnea,

mucocutaneous pallor,

. . .

), while clinical signs of hemolysis were

very inconsistent. The mean hemoglobin level was 7.6 g / dl. No

thrombocytopenia was associated; two hyperlymphocytosis were

found. Haptoglobin was reduced for 5 patients, normal in the

other two patients. Other biological hemolysis parameters were

inconsistent. The blood smear found for all patients anisocytosis;

no schistocyte is found (missing: 3). The Coombs test was positive

for all patients: 4 patients had a mixed profile (IgG + C3d); 2 had

a positive Coombs test type IgG alone, and only one patient had a

positive Coombs test type C3d alone. 3 patients had cold agglutinins

(cold hemagglutinin disease). The etiological assessment found 4

cases of lymphoma, one case of chronic lymphocytic leukemia, one

case of unclassified dysimmunity and idiopathic case. 4 patients

received corticosteroid therapy (one patient was complicating with

lumbar shingles and diabetes imbalance). Cold-protection measures

have been advocated for 3 patients; immunosuppressive treatment

for a single patient. One patient had, during its evolution, an

association with idiopathic thrombocytopenic purpura; another

patient died.

Conclusions:

This disease is difficult to diagnose in the elderly,

because of its rarity; lymphoma and chronic lymphocytic leukemia

being the main causes to look in the elderly.

P-265

MGUS and dystrophy myeloma: blurred border

P. Panek

1

, A. Martin-Kleisch

1

, L. Babe

1

, J.-L. Novella

2

, A.-A. Zulfiqar

1

1

CHU Reims, Reims, France;

2

France

Objectives:

Monoclonal gammopathy of undetermined significance

is a benign entity but very little diagnosed in the elderly; atypical

cases are difficult to identify in the elderly.

Methods:

We illustrate this data by a clinical case.

Results:

A 89-year-old woman was hospitalized for fall without

loss of consciousness. Normochromic normocytic aplastic anemia

was detected. A serum protein electrophoresis showed an IgG

monoclonal band kappa to 13.2 g/L, associated with proteinuria

estimated at 266mg/24h. Urine immunofixation also found IgG

ú

and

l

. The assessment was completed by a myelogram showing

a plasma cell dystrophic inclusion estimated at 3%. A moderate

chronic renal failure of unknown etiology has been present for

one year. No hypercalcemia was found. Presence of two gaps

X-rays of the skull were detected. LDH increased at 512 IU/L

and high

b

2 microglobulin to 4.65mg/L. Oncogeriatric assessment

found risk of malnutrition, mixed dementia pathology moderate

stage, a high risk of falls, a Cornell index 7/38 not in favor of

a depression. Haematological advice was requested, concluding

to a MGUS because only 3% of dystrophic plasma cells, but a

dystrophy myeloma was not excluded. No therapeutic was expected

because of her general condition and its comorbidities (colon cancer

with discharge stoma, in remission since 2001, and discovery

of a bilateral pulmonary embolism during her hospitalization).

Biological monitoring was recommended.

Conclusions:

Atypical aspects in the elderly raise the problem of

medical care, conditioned by an accurate evaluation oncogeriatric.

Geriatric rehabilitation

P-266

Three different outcomes in older patients receiving

intermediate care in nursing home after acute hospitalization

J.F. Abrahamsen

Storetveit Nursing homeMunicipality of Bergen and Kavli

forskningssenter for Geriatri og Demens, HDS, Bergen, Norway

Objectives:

To evaluate the recovery and outcome of older

community-dwelling patients admitted to intermediate care (IC) in

nursing home after acute hospitalization, and to compare patients

who were able and unable to return directly to their own homes.

Patients and Methods:

A prospective, observational, cohort study

conducted between June 2011 and 2014 in a 19-bed IC nursing

home ward with increased multidisciplinary staffing. A total of 961

community-dwelling patients, ≥70 years of age, considered to have

a rehabilitation potential and no major cognitive impairment or

delirium, transferred from internal medicine, cardiac, pulmonary

and orthopaedic hospital departments were included.