Maria Patricia Roman

Dr. Maria Patricia Roman

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Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 February 2020 in Neurourology and Urodynamics
Verified
Journal Article
Closed access
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MRMaria Patricia Roman
Maria Patricia Roman
SJStephanie Jones
Stephanie Jones
GFGabriele Falconi
Gabriele Falconi
JHJorge Milhem Haddad
Jorge Milhem Haddad
CBCornelia Betschart
Cornelia Betschart
SDStergios K. Doumouchtsis
Stergios K. Doumouchtsis

17 January 2023 in Medicina
Verified
Journal Article
Open access
PDF file
CBCarmen Elena Bucuri
Carmen Elena Bucuri
DMDan Mihu
Dan Mihu
DCDelia Clinciu
Delia Clinciu
VOValentin Oprea
Valentin Oprea
CBCostin Berceanu
Costin Berceanu
RCRazvan Ciortea
Razvan Ciortea
Abdominal cystic masses are diagnosed during the intrauterine period and have a relatively low incidence. Fetal ovarian cysts are the most common form diagnosed prenatally or immediately after birth. The pathophysiology of the development of these types of tumors is not fully elucidated, with ovarian hyperstimulation caused by maternal and placental hormones being the most accepted hypothesis. During intrauterine development, the diagnosis of fetal ovarian cysts is most often made accidentally during usual check-up ultrasounds corresponding to the first, second, and third trimesters of pregnancy. We conducted a scoping review with the aim to map the current knowledge regarding the treatment of fetal ovarian cysts diagnosed in the intrauterine period. Focusing on the articles published in the last 10 years in the specialized literature, we tried to identify a conceptualization regarding the surveillance and treatment of these anomalies.

5 September 2024 in Current Oncology
Verified
Journal Article
Open access
PDF file
CBCarmen Elena Bucuri
Carmen Elena Bucuri
RCrazvan ciortea
razvan ciortea
AMAndrei Mihai Malutan
Andrei Mihai Malutan
VOValentin C Oprea
Valentin C Oprea
MTMihai Toma
Mihai Toma
DMDan Mihu
Dan Mihu
Smooth Muscle Tumor of Uncertain Malignant Potential (STUMP) is a rare uterine tumor primarily affecting perimenopausal and postmenopausal women, typically aged between 45 and 55 years. Characterized by ambiguous histological features, STUMPs present diagnostic challenges as they cannot be definitively classified as benign or malignant based on morphology alone. This systematic review aims to elucidate the clinical, pathological, immunohistochemical, and treatment-related characteristics of STUMPs through an analysis of the literature from the past 20 years. The study follows PRISMA guidelines, utilizing comprehensive searches of PubMed and Scopus databases, yielding 32 studies that meet the inclusion criteria. From the analysis of these studies, it was revealed that the clinical presentations vary from common symptoms such as abnormal uterine bleeding and pelvic pain to incidental detection of uterine mass. Histologically, STUMPs demonstrate features overlapping with both leiomyomas and leiomyosarcomas, including mild nuclear atypia, low mitotic indices, and focal necrosis. Immunohistochemical markers such as p16 and p53 have been investigated for prognostic significance. Elevated p16 expression, often associated with aggressive behavior, was observed in a subset of STUMPs. Surgical management, typically involving hysterectomy or tumorectomy, is the primary treatment, though the extent of resection is variable. Adjuvant therapies are not routinely recommended, but long-term surveillance is advised, especially for high-risk patients. Recurrence rates for STUMPs are approximately 12%, with factors such as high mitotic counts and coagulative necrosis indicating higher risk. This review highlights the complexity of STUMP diagnosis and management, emphasizing the need for more precise diagnostic criteria and individualized treatment strategies. Understanding the morphological, immunohistochemical, and clinical behavior of STUMPs can improve patient outcomes and guide future research in this diagnostically challenging area.

3 August 2024 in Biomedicines
Verified
Journal Article
Open access
PDF file
CBCarmen Elena Bucuri
Carmen Elena Bucuri
RCrazvan ciortea
razvan ciortea
DCDelia Clinciu
Delia Clinciu
VOValentin C Oprea
Valentin C Oprea
MTMihai Toma
Mihai Toma
DMDan Mihu
Dan Mihu
Disseminated peritoneal leiomyomatosis (DPL) is a rare condition marked by multiple leiomyomas in the peritoneal cavity, predominantly affecting women of reproductive age. Although typically benign, DPL can present significant diagnostic challenges and, in rare cases, may progress to malignancy. A primary contributing factor to DPL is iatrogenic, particularly due to surgical interventions such as morcellation during myomectomy. This scoping review explores the pathogenesis, epidemiology, diagnosis, and management of DPL, highlighting the crucial role of hormonal influences and iatrogenic factors. Diagnostic methods include computed tomography, ultrasound, magnetic resonance imaging, and histopathological evaluation, which are essential for assessing disease extent and guiding treatment. Management strategies encompass surgical intervention—with a focus on minimizing iatrogenic risks—conservative approaches for asymptomatic patients, and advancements in hormonal treatments. Emphasis is placed on preventing iatrogenic dissemination through refined surgical techniques and patient education. Despite its rarity, with fewer than 200 cases reported globally, understanding DPL’s clinical presentation and iatrogenic origins is vital for optimal patient outcomes. This review underscores the importance of early diagnosis, personalized treatment plans, and ongoing research to address the challenges associated with DPL.

26 June 2020 in BMC Pregnancy and Childbirth
Verified
Journal Article
Open access
PDF file
SDStergios K. Doumouchtsis
Stergios K. Doumouchtsis
MRMaria Patricia Roman
Maria Patricia Roman
Vasilios PergialiotisVasilios Pergialiotis
Vasilios Pergialiotis
GFGabriele Falconi
Gabriele Falconi
JHJorge Milhem Haddad
Jorge Milhem Haddad
CBCornelia Betschart
Cornelia Betschart
Background: More than 85% of women sustain different degrees of trauma during vaginal birth. Randomized controlled trials on childbirth pelvic floor trauma have reported a wide range of outcomes and used different outcome measures. This variation restricts effective data synthesis, impairing the ability of research to inform clinical practice. The development and use of a core outcome set (COS) for childbirth pelvic floor trauma aims to ensure consistent use of outcome measures and reporting of outcomes. Methods: An international steering group, within CHORUS, an International Collaboration for Harmonising Outcomes, Research and Standards in Urogynaecology and Women’s Health, including academic community members, researchers, healthcare professionals, policy makers and women with childbirth pelvic floor trauma will lead the development of this COS. Relevant outcome parameters will be identified through comprehensive literature reviews. The selected outcomes will be entered into an international, multi-perspective online Delphi survey. Subsequently and based on the results of the Delphi surveys consensus will be sought on ‘core’ outcomes. Discussion: Dissemination and implementation of the resulting COS within an international context will be supported and promoted. Embedding the COS for childbirth pelvic floor trauma within future clinical trials, systematic reviews, and clinical practice guidelines is expected to enrich opportunities for comparison of future clinical trials and allow better synthesis of outcomes, and will enhance mother and child care. The infrastructure created by developing a COS for childbirth pelvic floor trauma could be leveraged in other settings, for example, advancing research priorities and clinical practice guideline development.

11 September 2023 in European Journal of Obstetrics & Gynecology and Reproductive Biology
Verified
Journal Article
Closed access
MRMaria Patricia Roman
Maria Patricia Roman
SAShaurya Aggarwal
Shaurya Aggarwal
SDStergios K. Doumouchtsis
Stergios K. Doumouchtsis