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4. Hrvatski kongres kliniËke citologije 4th Croatian Congress ... - Penta

4. Hrvatski kongres kliniËke citologije 4th Croatian Congress ... - Penta

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Clinical Cytology - Posters<br />

NEONATAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS - CASE REPORT<br />

Roganović J1 , Kvenić B1 , Jonjić N2 , Seili-Bekafigo I3 , Kardum-Skelin I4 1Division of Hematology and Oncology, University Children’S Hospital Rijeka;<br />

2Department of Pathology, School of Medicine Rijeka;<br />

3Department of Cytology, Department of Internal Medicine,<br />

Clinical Hospital Centar Rijeka, Croatia<br />

4Laboratory for Hematology and Cytology, Clinical Hospital Merkur, Zagreb, Croatia<br />

Hemophagocytic lymphohystiocytosis (HLH) represents a severe hyperinflammatory<br />

condition with the cardinal symptoms prolonged fever, hepatosplenomegaly, and cytopenias.<br />

The most prominent histopathological feature is an accumulation of activated<br />

T lymphocytes and macrophages predominantly in lymphoid tissues. Although it can occur<br />

in all age groups, neonatal-onset HLH is very rare. We report on a case of HLH presenting<br />

with anemia and respiratory distress at birth. Several weeks prior to diagnosis<br />

the symptoms were attributed to a systemic infection. The child developed typical clinical<br />

and laboratory findings, and was diagnosed with HLH according to the HLH-2004 guidelines.<br />

Chemo-immunotherapy was initiated, but after a temporary control of the disease<br />

he succumbed to rapidly progressive HLH. Post-mortem, extensive hemophagocytosis<br />

was found in multiple organs. No specific genetic defect was identified.<br />

HLH is potentially fatal childhood disease. It is important for pediatricians to be able<br />

to early identify this disorder and commence the therapy before overwhelming disease<br />

activity develops.<br />

jelena.roganovic1@ri.t-com.hr<br />

EOSINOPHILIC MASTITIS: A CASE REPORT OF AN EOSINOPHILIC MASTITIS IN<br />

A 32-YEAR OLD FEMAL<br />

Ropar S1 , Gredelj Šimec NJ2 , Tokić T2 1General Hospital Karlovac, Department for cytology, Karlovac, Croatia<br />

2General Hospital Karlovac, Department of Internal Medicine, Karlovac, Croatia<br />

Eosinophilic mastitis is a rare entity and mainly connected with significant eosinophilia<br />

in peripheral blood. We have presented a case of eosinophilic mastitis which appeared<br />

in a 32-year old female patient after unusually intense exposure to house dust. The disease<br />

has manifested itself with redness and itching of the skin of both breasts, bilateral<br />

retromamilar nodes painful to palpation, same as dense secretion from both breasts.<br />

The cytological analysis of the breast’s secretion, same as the aspirate of a nodule of the<br />

breast has shown numerous eosinophils, some phagocytes and numerous eosinophilic<br />

granules. Eosinophilia was also present in the blood. Allergy against house dust was<br />

proven with cutaneous prick test. A therapy with antihistamines led to total regression<br />

of symptoms, same as to normalisation of laboratory results which convinced us in addition<br />

that the case was related to eosinophilic mastitis.<br />

samija66@gmail.com<br />

137<br />

4 th <strong>Croatian</strong> <strong>Congress</strong> of Clinical Cytology / 1 st <strong>Croatian</strong> Symposium of Analytical Cytology / 2 nd <strong>Croatian</strong> Symposium of Cytotechnology

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