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    <title>DSpace Collection:</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/33046</link>
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    <dc:date>2026-09-04T20:39:38Z</dc:date>
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  <item rdf:about="http://repository.usmf.md:80/handle/20.500.12710/33579">
    <title>“Ankylosing spondylitis – an old disease with new perspectives”. Author: Lia Chișlari, MD, PhD, associate professor</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/33579</link>
    <description>Title: “Ankylosing spondylitis – an old disease with new perspectives”. Author: Lia Chișlari, MD, PhD, associate professor
Authors: Revenco, Ninel</description>
    <dc:date>2026-01-01T00:00:00Z</dc:date>
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  <item rdf:about="http://repository.usmf.md:80/handle/20.500.12710/33577">
    <title>Professor Valeriu Revenco at 70 – a life dedicated to excellence in cardiology</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/33577</link>
    <description>Title: Professor Valeriu Revenco at 70 – a life dedicated to excellence in cardiology
Authors: Grib, Livi</description>
    <dc:date>2026-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://repository.usmf.md:80/handle/20.500.12710/33557">
    <title>Proteus syndrome in a young African woman: a clinically diagnosed ultra-rare mosaic overgrowth disorder</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/33557</link>
    <description>Title: Proteus syndrome in a young African woman: a clinically diagnosed ultra-rare mosaic overgrowth disorder
Authors: Voloc, Chiril; Olaru, Andrei; Rusu, Irina; Revenco, Ninel; Voloc, Alexandru
Abstract: Proteus syndrome is an extremely rare congenital multisystem disorder characterized by highly variable clinical manifestations.&#xD;
Its exact prevalence remains unknown, with fewer than 200 cases reported in the medical literature worldwide.&#xD;
Clinical case description. We report the case of an 18-year-old African woman diagnosed with Proteus syndrome, presenting&#xD;
with marked asymmetrical overgrowth affecting the upper limbs, trunk, and lower limbs. The distribution of the&#xD;
deformities resembled the appearance of a tree trunk with multiple stumps. Additionally, the patient exhibited soft tissue&#xD;
tumor-like formations at the left oral commissure and in the left retroauricular region.&#xD;
Conclusion. The detailed phenotypic description of individuals with Proteus syndrome is essential due to the extreme&#xD;
rarity and clinical complexity of this disorder. Improved awareness and diagnostic acumen among healthcare professionals&#xD;
are critical for the early identification and appropriate multidisciplinary management of affected patients. Given the&#xD;
high risk of life-threatening complications, such as the development of malignant tumors and thromboembolic events, a&#xD;
structured and dynamic follow-up protocol is required. Moreover, the psychosocial dimension of the disease must not be&#xD;
overlooked. Many patients experience profound emotional distress, stigmatization, and moral suffering, which can significantly&#xD;
impact their quality of life. An integrated approach that combines medical surveillance with psychological and social&#xD;
support is imperative for optimizing long-term outcomes in Proteus syndrome.</description>
    <dc:date>2026-01-01T00:00:00Z</dc:date>
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  <item rdf:about="http://repository.usmf.md:80/handle/20.500.12710/33556">
    <title>Psoriasis vulgaris and B-cell non-Hodgkin lymphoma: a complex case with rare cephalic localization</title>
    <link>http://repository.usmf.md:80/handle/20.500.12710/33556</link>
    <description>Title: Psoriasis vulgaris and B-cell non-Hodgkin lymphoma: a complex case with rare cephalic localization
Authors: Rotari, Mihaela; Bețiu, Mircea; Buruiană, Sanda; Pînzaru, Valeria; David, Valeriu; Șaptefrați, Lilian
Abstract: Introduction. Psoriasis is a chronic immune-mediated inflammatory condition and is considered a potential risk factor&#xD;
for the development of hematologic malignancies, particularly in the context of immunosuppressive therapy and T-cell&#xD;
dysfunction. B-cell non-Hodgkin lymphomas are neoplasms of the lymphatic system with variable clinical manifestations,&#xD;
most commonly presenting with peripheral lymphadenopathy. Primary localization in the soft tissues of the head, with&#xD;
bone invasion, is rare.&#xD;
Case presentation. We report a rare case of cephalic aggressive NHL Not Otherwise Specified (NOS) in a 63-year-old&#xD;
patient with a history of psoriasis vulgaris and Clear cell carcinoma (T1N0M0, treated in 2021 at the Oncology Institute&#xD;
in Chișinău), who presented with a painless right temporo-parietal mass. MRI revealed a 48×19×50 mm lesion in the&#xD;
temporal soft tissues with extension into the frontal bone. Surgical biopsy and immunohistochemistry (CD20+, CD79a+,&#xD;
CD45+, BCL6-) confirmed the diagnosis of B-cell NHL NOS. In 2022, the patient received 8 induction cycles of immunochemotherapy&#xD;
followed by maintenance therapy with Rituximab. PET/CT evaluation showed a Deauville score of 3, indicating&#xD;
a partial favorable response. Associated comorbidities (psoriasis, type 2 diabetes mellitus, hypertension) required multidisciplinary&#xD;
monitoring.&#xD;
Conclusions. This case illustrates an unusual cranial localization of aggressive B-cell lymphoma NOS and highlights the&#xD;
potential link between psoriasis and lymphoproliferative risk, as previously suggested in the medical literature.</description>
    <dc:date>2026-01-01T00:00:00Z</dc:date>
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