Mihai Popescu

Mihai Popescu

*This is an algorithmically generated author record based on publicly available information.

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Mihai Popescu has a total of 43 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Radiotherapy in Squamous Cell Carcinoma of the Lip: A Systematic Review of Reported Practices, Clinical Outcomes, and Gaps in Consensus

    by Oana Ciobănescu, Anda Elena CrișAn, Răzvan Marian Bălan, Virgil PătrașCu, Andrada-Nemesis CrișAn, Cristiana-Iulia Dumitrescu, Mădălin-Cristian Moraru, Suzana Măceș, Mihai Popescu, Daniela Dumitrescu

    Background/Objectives: Squamous cell carcinoma (SCC) of the lip occupies an ambiguous position between cutaneous and oral-cavity oncology and lacks dedicated radiotherapy guidelines, resulting in considerable practice variability. We systematically reviewed the reported radiotherapy practices, clinical outcomes and gaps in consensus at this site. Methods: Following PRISMA 2020 and prospectively registered in PROSPERO (CRD420261349994), we searched PubMed/MEDLINE, Scopus, the Cochrane Library (Trials) and ClinicalTrials.gov (20 March 2026). Studies of at least ten patients with lip SCC treated with external beam radiotherapy or brachytherapy were eligible. Risk of bias was assessed with ROBINS-I; the synthesis was narrative, following the Synthesis Without Meta-analysis (SWiM) reporting framework. Results: Nine studies (approximately 3904 patients; 1964–2021; six countries) met the criteria. Interstitial brachytherapy was the dominant modality (seven studies), with high local control (approximately 93–97% in modern actuarial series), favourable toxicity and good functional/aesthetic outcomes; external beam radiotherapy served mainly as adjuvant treatment. Doses, fractionation, nodal management and outcome reporting were markedly heterogeneous, and eight of nine studies were at serious risk of bias. Conclusions: Radiotherapy—in the identified literature, in effect, largely historical interstitial brachytherapy—appears to be an effective, organ-preserving option in early-stage lip SCC; no conclusions can be drawn for modern external beam techniques such as IMRT. The limited, brachytherapy-dominated evidence warrants cautious interpretation and justifies protocol standardisation, a core outcome set with validated quality-of-life instruments, and multi-institutional prospective registries.

  • Open Access

    Spermatocytic Tumor Arising in a Cryptorchid Testis: A Case Report and Narrative Review

    by Laurențiu Augustus Barbu, Stelian-Stefaniță Mogoantă, Liliana Cercelaru, Marius Cristian Marinaș, Nicolae-Dragoș Mărgăritescu, Mihai Popescu, Valentina Căluianu, Gabriel Florin Răzvan Mogoș, Liviu Vasile, Tiberiu Stefăniță Țenea Cojan

    Background: Spermatocytic tumor (ST) is a rare non-GCNIS-derived testicular germ cell neoplasm that predominantly affects older men and generally follows an indolent course. Its occurrence in a cryptorchid testis is exceptionally uncommon. Methods: A narrative literature review was conducted using the PubMed database, including studies published up to August 2026. The search used combinations of the terms “spermatocytic tumor”, “spermatocytic seminoma”, “cryptorchidism”, “undescended testis”, “immunohistochemistry”, “molecular features”, “magnetic resonance imaging”, and “treatment”. Results: A 56-year-old man presented with a painless left inguinal mass corresponding to a cryptorchid testis. Serum tumor markers were normal. MRI demonstrated a well-circumscribed heterogeneous lesion with pseudocystic areas and enhancement of the solid component. Radical inguinal orchiectomy was performed. Histopathological examination revealed the characteristic triphasic cellular population without GCNIS, lymphovascular invasion, or sarcomatous transformation. Immunohistochemistry showed SALL4 and CD117 positivity and absence of OCT3/4 and D2-40 expression, supporting the diagnosis of ST and its distinction from classical seminoma. No recurrence or metastatic disease was detected during 12 months of follow-up. Conclusions: ST arising in a cryptorchid testis represents an exceptionally uncommon presentation. Integration of clinical, radiological, morphological, and immunohistochemical findings is essential for accurate diagnosis and distinction from classical seminoma, thereby avoiding unnecessary additional treatment.

  • Open Access

    Platform-Dependent Differences in Beam Characteristics and Low-Dose Exposure: A Comparative Study of Elekta™ Synergy and Varian TrueBeam™ Linear Accelerators Using SunSCAN™ 3D Phantom and Octavius® 4D QA

    by Marian-Răzvan Bălan, Anda Elena CrișAn, Eugen Osiac, Cristiana-Iulia Dumitrescu, Suzana Măceș, Mihai Popescu, Luana Corina Lascu, Maria Mihai, Sanda-Amelia Drăcea, Oana Ciobănescu, et al.

    Background/Objectives: Inter-platform variability in beam characteristics and low-dose exposure may arise from differences in linear accelerator head design, multileaf collimator geometry, and dose calculation algorithms. This study aimed to evaluate system-level dosimetric differences between two widely used linear accelerator platforms under clinically commissioned conditions. Methods: A comparative dosimetric analysis was performed between Elekta Synergy and Varian TrueBeam linear accelerators. Beam data were acquired using a SunSCAN™ 3D water phantom, and patient-specific quality assurance was conducted with the Octavius® 4D system. Treatment plans were generated for left-sided breast, prostate, and head and neck cases using clinically commissioned treatment planning systems. Beam flatness, symmetry, penumbra width, low-dose exposure, conformity, homogeneity, and organ-at-risk dose metrics were evaluated. Results: Platform-dependent differences were observed in penumbra behavior and out-of-field dose, primarily attributable to intrinsic linac head design and collimation characteristics. These differences propagated into clinical plans, with greater variability observed for breast and head and neck cases, while prostate plans showed higher consistency between platforms. Algorithm-dependent trends were noted for conformity and homogeneity indices; however, all plans met institutional clinical acceptance criteria during quality assurance. Stricter gamma evaluation criteria revealed systematic but limited inter-platform deviations. Conclusions: Elekta Synergy and Varian TrueBeam demonstrated clinically acceptable dosimetric performance, with modest platform-dependent differences. While target coverage and overall plan quality were comparable, these variations were primarily observed in peripheral dose regions and may be relevant for platform-specific planning optimization and quality assurance. This supports the importance of comprehensive commissioning and QA procedures in both mixed- and single-platform clinical settings, particularly for highly modulated techniques.

  • Open Access

    Semi-Automated Lung Segmentation Based on Region-Growing Methods in Interstitial Lung Disease

    by Mădălin-Cristian Moraru, Cristiana-Iulia Dumitrescu, Suzana Măceș, Cătălin Ciobîrcă, Mihai Popescu, Luana Corina Lascu, Dragoș-Ovidiu Alexandru, Diana-Maria Trască, Diana Maria Ciobîrcă, Marian-Răzvan Bălan, et al.

    Background: One of the main tools for investigating pulmonary disorders is computed tomography. Starting with a CT, analyses can be qualitative (e.g., direct interpretation of 2D slices, virtual bronchoscopy) or quantitative (e.g., fibrosis score). Qualitative analyses can be performed without segmentation, but quantitative analyses require lung segmentation. Methods: We present the concepts for a class of lung segmentation methods that use region-growing algorithms, the implementation and testing details, and the results obtained in our software platform. Accurate segmentation of lung regions from medical images is a crucial step in computer-aided diagnosis (CAD) systems for pulmonary diseases such as chronic obstructive pulmonary disease (COPD), pneumonia, and lung cancer. Manual segmentation is time-consuming and subjective, while fully automated methods may fail under challenging imaging conditions. Results: This article presents a semi-automated lung segmentation approach, based on region-growing methods, that balances automation with user control. Conclusions: The proposed technique effectively delineates lung boundaries in computed tomography (CT), minimizing computational complexity and manual effort.


  • Open Access

    Serous Papillary Adenofibroma Cyst of the Ovary in a Young Woman: Case Report and Literature Review

    by Laurențiu Augustus Barbu, Liliana Cercelaru, Valeriu Șurlin, Stelian-Stefaniță Mogoantă, Tiberiu Stefăniță Țenea Cojan, Nicolae-Dragoș Mărgăritescu, Ana-Maria Țenea Cojan, Mihai Popescu, Valentina Căluianu, Gabriel Florin Răzvan Mogoș, et al.

    Background: Serous papillary adenofibroma cyst (SPAC) of the ovary is a rare benign epithelial tumor that can mimic borderline or malignant ovarian neoplasms. Reports in young women are particularly scarce. Purpose: The aim of this study is to present a rare clinical case of ovarian SPAC in a young woman and to review the existing literature, highlighting diagnostic challenges and implications for fertility-preserving management. Methods: We present a clinical case of ovarian SPAC in a 41-year-old woman and conducted a narrative literature review. The search was performed in PubMed, Scopus, and Web of Science to identify reports published between 2000 and 2025. Additional relevant articles were also identified through manual screening of reference lists from selected papers. Results: MRI revealed a well-encapsulated septated cystic lesion with solid nodular components and post-contrast enhancement. Tumor markers, including CA 19-9, were elevated. Laparoscopic surgery with intraoperative frozen section confirmed the diagnosis of SPAC, allowing fertility-preserving management. Histopathology established the final diagnosis. Conclusions: This case emphasizes the importance of considering SPAC in the differential diagnosis of complex adnexal masses. Early recognition and intraoperative frozen section can guide conservative surgical strategies, avoiding overtreatment and preserving reproductive potential in young patients.


  • Open Access

    Enteroenteric Fistula Following Multiple Magnet Ingestion in an Adult: Case Report, Literature Review and Management Algorithm

    by Laurențiu Augustus Barbu, Liliana Cercelaru, Ionică-Daniel Vîlcea, Valeriu Șurlin, Stelian-Stefaniță Mogoantă, Tiberiu Stefăniță Țenea Cojan, Nicolae-Dragoș Mărgăritescu, Ana-Maria Țenea Cojan, Valentina Căluianu, Mihai Popescu, et al.

    Background: Multiple high-powered magnet ingestion is a surgical emergency due to inter-loop attraction leading to ischemia, necrosis, perforation, and fistula formation. While well documented in children, adult cases—particularly those complicated by entero-enteric fistula—remain rare, and management is largely extrapolated from pediatric guidelines. Objective: To present a rare case of adult entero-enteric fistula following multiple neodymium magnet ingestion, we review the literature and propose an adapted management algorithm for adults. Methods: A narrative PubMed review was performed to identify pediatric and adult cases of magnet ingestion complicated by gastrointestinal fistula. Search terms included magnet ingestion, entero-enteric fistula, neodymium, and adult. Reported case characteristics, diagnostic modalities, treatments, and outcomes were analyzed. Results: A 38-year-old male with schizophrenia presented with small bowel obstruction five days after ingesting multiple magnets. Abdominal radiography revealed clustered radiopaque bodies in the distal ileum. Emergency laparotomy identified an entero-enteric fistula caused by pressure necrosis from inter-loop magnetic attraction. Segmental enterectomy with side-to-side anastomosis was performed, with uneventful recovery. The literature review identified only a few adult cases, which showed similar pathophysiology but frequent diagnostic delays and higher complication rates compared with pediatric cases. Conclusions: This case adds to the scarce adult literature on magnet-induced entero-enteric fistula and supports the adaptation of pediatric-based protocols for adults, with attention paid to psychiatric comorbidity and delayed presentation. Early imaging, timely intervention, and multidisciplinary care are essential to prevent severe gastrointestinal injury.


  • Open Access

    Coexistence of Acute Appendicitis and Mesenteric Cystic Lymphatic Malformation in an Adult: A Case Report and Narrative Review of Intraoperative Management Strategies

    by Laurențiu Augustus Barbu, Liliana Cercelaru, Ionică-Daniel Vîlcea, Valeriu Șurlin, Stelian-Stefaniță Mogoantă, Tiberiu Stefăniță Țenea Cojan, Nicolae-Dragoș Mărgăritescu, Mihai Popescu, Gabriel Florin Răzvan Mogoș, Liviu Vasile

    Background: Mesenteric cystic lymphatic malformations (MCLMs) are rare benign lymphatic malformations predominantly diagnosed in children. Adult cases are exceptional and typically discovered incidentally during imaging or surgery for unrelated conditions. Their intraoperative identification, particularly in emergency settings, poses diagnostic and surgical challenges due to anatomical complexity and potential vascular involvement. Methods: A literature review was performed in PubMed and Scopus to contextualize this case, focusing on intraoperative management strategies, recurrence risk, and surgical decision-making in mesenteric lymphatic malformations. Case reports, case series, and reviews in English with relevant clinical and surgical data were included, while duplicates, non-English publications, abstracts without full text, and studies lacking essential information were excluded. Case Presentation: We report a 45-year-old male who presented with acute right lower quadrant pain, clinically and radiologically consistent with acute appendicitis. Contrast-enhanced CT incidentally identified a mesenteric cystic lesion near the terminal ileum. Intraoperative findings confirmed phlegmonous appendicitis coexisting with a large MCLM, requiring segmental enterectomy and appendectomy. Histopathology confirmed the diagnosis of MCLMs. Conclusions: This case highlights the rare coexistence of acute appendicitis and mesenteric lymphatic malformations in an adult, illustrating the surgical challenges of unexpected lymphatic lesions in emergency settings. Emphasizing real-time intraoperative decision-making, we propose an anatomy-driven algorithm that balances complete excision with safer, conservative options based on lesion features, surgical risk, and multidisciplinary input.


  • Open Access

    Small Bowel Tumors: A 7-Year Study in a Tertiary Care Hospital

    by Sergiu Marian Cazacu, Dan Cârțu, Mihai Popescu, Liliana Streba, Bogdan Silviu Ungureanu, Vlad Florin Iovănescu, Mihai Cimpoeru, Cecil Sorin Mirea, Valeriu Marian Surlin, Stelian Mogoantă, et al.

    (1) Background: Tumors of the small bowel represent 3–6% of gastrointestinal neoplasms and 3–6% of GI malignancies. The difficulties regarding the diagnosis are associated with larger tumors at the moment of the diagnosis and with advanced forms of malignant tumors, associated with a dismal prognosis. (2) Methods: We performed an observational, retrospective, cohort study that included patients with small bowel tumors admitted to the Craiova County Emergency Clinic Hospital between 1 January 2017 and 31 December 2023. The data were collected from the analysis of the patient’s discharge documents from the Hippocrates computer system of the hospital and the evaluation of endoscopy databases. Patients under 16 years of age, those with no pathological confirmation of the malignancy, and those with insufficient data were excluded. (3) Results: A total of 80 cases of small bowel tumors were diagnosed; 72.5% were malignant, of which 10.3% were metastases. The most frequent primary malignant small bowel tumor was adenocarcinoma; two squamous cell carcinomas were noted. CT scans and upper digestive endoscopy represent the most frequent imaging methods for the diagnosis. The prognosis for malignant tumors was poor, with a 41% 5-year survival rate. (4) Conclusions: Small bowel tumors are rarely encountered, with 72.5% being malignant, and were diagnosed at large dimensions and in advanced stages for malignant tumors, with a dismal prognosis.