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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">akusherstvo</journal-id><journal-title-group><journal-title xml:lang="en">Obstetrics, Gynecology and Reproduction</journal-title><trans-title-group xml:lang="ru"><trans-title>Акушерство, Гинекология и Репродукция</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2313-7347</issn><issn pub-type="epub">2500-3194</issn><publisher><publisher-name>IRBIS LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.17749/2313-7347/ob.gyn.rep.2026.677</article-id><article-id custom-type="elpub" pub-id-type="custom">akusherstvo-2718</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL CASE</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>КЛИНИЧЕСКИЙ СЛУЧАЙ</subject></subj-group></article-categories><title-group><article-title>Role of modern ultrasonography in antenatal detection of placenta increta: a case report</article-title><trans-title-group xml:lang="ru"><trans-title>Роль современной ультрасонографии в антенатальной диагностике врастания плаценты: клинический случай</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5175-2689</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Элиава</surname><given-names>Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Eliava</surname><given-names>E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Элиава Екатерина</p><p>Scopus Author ID: 57205196899</p><p>0159 Тбилиси, Люблянская ул., д. 12; 4100 Сенаки, ул. Чкондидели, д. 13</p></bio><bio xml:lang="en"><p>Ekaterine Eliava, MD</p><p>Scopus Author ID: 57205196899</p><p>66 Lubliana Str., 0159 Tbilisi; 13 Chkondideli Str., Senaki 4100</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8110-5485</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Верулава</surname><given-names>Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Verulava</surname><given-names>T.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Верулава Тенгиз - д.м.н., проф.</p><p>Scopus Author ID: 56602860500</p><p>0102 Тбилиси, ул. Пааты Саакадзе, д. 1; 3000 Мельбурн, ул. Ла Троуб, д. 124</p></bio><bio xml:lang="en"><p>Tengiz Verulava, MD, Dr Sci Med, Prof.</p><p>Scopus Author ID: 56602860500</p><p>1 Paata Saakadze Str., 0102 Tbilisi; 124 La Trobe Street Melbourne 3000</p></bio><email xlink:type="simple">tverulava@cu.edu.ge</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Национальный медицинский центр имени академика О. Гудушаури; Медицинский центр Западной Грузии «Сенамеди»</institution><country>Грузия</country></aff><aff xml:lang="en"><institution>Academician O. Ghudushauri National Medical Center; Senamedi West Georgia Medical Center</institution><country>Georgia</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Кавказский университет; Королевский Мельбурнский технологический институт</institution><country>Грузия</country></aff><aff xml:lang="en"><institution>Caucasus University; Royal Melbourne Institute of Technology</institution><country>Georgia</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2026</year></pub-date><pub-date pub-type="epub"><day>12</day><month>03</month><year>2026</year></pub-date><volume>20</volume><issue>1</issue><fpage>220</fpage><lpage>228</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Eliava E., Verulava T., 2026</copyright-statement><copyright-year>2026</copyright-year><copyright-holder xml:lang="ru">Элиава Е., Верулава Т.</copyright-holder><copyright-holder xml:lang="en">Eliava E., Verulava T.</copyright-holder><license license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.gynecology.su/jour/article/view/2718">https://www.gynecology.su/jour/article/view/2718</self-uri><abstract><sec><title>Introduction</title><p>Introduction. The rising global incidence of cesarean deliveries has led to elevated abnormal placentation, particularly placenta accreta spectrum (PAS) disorders. These conditions represent serious obstetric complications with high risks for both maternal and fetal morbidity and mortality.</p></sec><sec><title>Аim</title><p>Аim: to analyze a clinical case of placenta increta with deep invasion, highlighting the diagnostic value of advanced ultrasonographic techniques.</p></sec><sec><title>Case presentation</title><p>Case presentation. A 29-year-old pregnant woman with a history of three cesarean sections (2014, 2017, and 2025) and prominent somatic comorbidities (chronic pyelonephritis and urolithiasis) underwent routine antenatal ultrasound screenings at 8, 12, 20, 23, and 28+6 weeks of gestation. Standard transvaginal and transabdominal sonographic techniques were used. After sonographic suspicion of placenta increta, magnetic resonance imaging (MRI) was performed for verification. Final diagnosis was confirmed intraoperatively and through histopathological analysis. Ultrasound revealed signs consistent with PAS type 2 (placenta increta): marked thinning of the myometrium, dilated lacunae, retroplacental hypervascularization, and placental bulging. At 28+6 weeks, transvaginal sonography detected further invasion into the cervical canal (PAS 3a). Color Doppler imaging revealed vascular "rail signs," indicating deep invasion. MRI confirmed complete placenta previa with abnormal tissue growth into the uterine scar and myometrial layers. This case demonstrates the effectiveness of modern ultrasonography and Doppler imaging in the early identification and classification of PAS disorders. Although previous publications emphasized limitations in determining invasion depth via ultrasound, this report highlights its diagnostic reliability, especially when complemented by MRI. Early diagnosis is essential for surgical planning and improving perinatal outcomes.</p></sec><sec><title>Conclusion</title><p>Conclusion. Ultrasound primarily combined with color Doppler imaging, provides a reliable and non-invasive means for diagnosing PAS disorders. In this case, the identification of specific Doppler features – particularly the "rail sign" representing vascular bridging between the myometrium and serosa – proved critical for diagnosing placenta increta. These findings highlight a potential for advanced Doppler markers in improving antenatal detection and surgical planning. Integrating such diagnostic techniques into routine care can markedly improve maternal and fetal outcomes in high-risk pregnancies.</p></sec></abstract><trans-abstract xml:lang="ru"><sec><title>Введение</title><p>Введение. Рост числа кесаревых сечений во всем мире привел к увеличению количества аномалий плацентации, в частности нарушений, связанных с приращением плаценты (ПП). Эти состояния представляют собой серьезные акушерские осложнения, сопряженные с высоким риском заболеваемости и смертности как матери, так и плода.</p></sec><sec><title>Цель</title><p>Цель: проанализировать клинический случай ПП с глубокой инвазией и подчеркнуть диагностическую ценность современных ультразвуковых методов.</p></sec><sec><title>Клинический случай</title><p>Клинический случай. 29-летняя беременная с тремя кесаревыми сечениями в анамнезе (в 2014, 2017 и 2025 гг.) и сопутствующими соматическими заболеваниями (хронический пиелонефрит и мочекаменная болезнь) прошла плановое дородовое ультразвуковое исследование (УЗИ) на 8, 12, 20, 23 и 28+6 неделях беременности. Использовались стандартные трансвагинальные и трансабдоминальные методы ультразвуковой диагностики. При подозрении на ПП по данным УЗИ для подтверждения была проведена магнитно-резонансная томография (МРТ). Окончательный диагноз был подтвержден во время операции и с помощью гистопатологического анализа. УЗИ выявило признаки, соответствующие ПП 2-го типа (placenta increta): выраженное истончение миометрия, расширенные лакуны, ретроплацентарная гиперваскуляризация и выпячивание плаценты. На сроке 28+6 недель трансвагинальное УЗИ выявило дальнейшее проникновение в цервикальный канал (предлежание плаценты 3а). Цветное доплеровское картирование выявило сосудистые «рельсы», указывающие на глубокое проникновение. МРТ подтвердила полное предлежание плаценты с аномальным разрастанием тканей в рубце на матке и в слоях миометрия. Этот случай демонстрирует эффективность современного УЗИ и доплерографии в ранней диагностике и классификации предлежания плаценты. Хотя в предыдущих публикациях подчеркивались ограничения в определении глубины инвазии с помощью УЗИ, в этом отчете подчеркивается его диагностическая надежность, особенно в сочетании с МРТ. Ранняя диагностика необходима для планирования хирургического вмешательства и улучшения перинатальных исходов.</p></sec><sec><title>Заключение</title><p>Заключение. УЗИ, особенно в сочетании с цветовым доплеровским картированием, является надежным и неинвазивным методом диагностики нарушений, связанных с ПП. В данном случае выявление специфических доплеровских признаков, в частности «рельсового знака», представляющего собой сосудистое соединение между миометрием и серозной оболочкой, сыграло решающую роль в диагностике ПП. Эти результаты подчеркивают потенциал современных доплеровских маркеров в улучшении пренатальной диагностики и планировании хирургического вмешательства. Внедрение таких методов диагностики в стандартную медицинскую практику может значительно улучшить состояние матери и плода при беременности с высоким риском.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>приращение плаценты</kwd><kwd>приращение плодного яйца</kwd><kwd>ультразвуковое исследование</kwd><kwd>доплерография</kwd><kwd>магнитно-резонансная томография</kwd><kwd>МРТ</kwd><kwd>кесарево сечение</kwd><kwd>аномальное прикрепление плаценты</kwd><kwd>материнская заболеваемость</kwd></kwd-group><kwd-group xml:lang="en"><kwd>placenta accreta spectrum</kwd><kwd>placenta increta</kwd><kwd>ultrasound</kwd><kwd>Doppler</kwd><kwd>magnetic resonance imaging</kwd><kwd>MRI</kwd><kwd>cesarean section</kwd><kwd>abnormal placentation</kwd><kwd>maternal morbidity</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Авторы заявляют об отсутствии финансирования</funding-statement><funding-statement xml:lang="en">The authors declare no funding</funding-statement></funding-group></article-meta></front><body><sec><title>Introduction / Введение</title><p>Placenta accreta is a severe pregnancy complication that occurs when placental tissue and blood vessels abnormally invade the uterine wall. The history of placenta accreta dates back more than a century. The earliest case documented in 1890 is reported from Tübingen, Germany, in 1890. Later, in 1937, C. Irving and A.T. Hertig published the first comprehensive case series, providing a systematic description and classification of abnormal placental adherence [<xref ref-type="bibr" rid="cit1">1</xref>]. While earlier single case reports existed, their work laid the foundation for clinical recognition and standardization of the diagnosis.</p><p>In recent years, the terminology and classification of this pathology was revised. The term Placenta Accreta Spectrum (PAS) is now globally accepted and encompasses a range of abnormal placental adherence and invasion, including placenta accreta, increta, and percreta [<xref ref-type="bibr" rid="cit2">2</xref>]. PAS disorders have become more prevalent alongside the global rise in cesarean deliveries, posing serious risks to both maternal and fetal health.</p></sec><sec><title>Etiological factors and risk stratification / Этиологические факторы и стратификация риска</title><p>PAS disorders are multifactorial in origin and are strongly associated with defective decidualization and excessive trophoblastic invasion. Normally, the decidua basalis provides a protective barrier that prevents chorionic villi from invading the myometrium. When this barrier lacks or underdeveloped, commonly due to previous uterine surgeries such as cesarean section, myomectomy, or curettage, the placenta may penetrate the myometrium pathologically [<xref ref-type="bibr" rid="cit3">3</xref>].</p><p>Established risk factors for PAS include:</p><p>These factors often overlap, increasing the overall risk. In the current case, the patient's history of multiple cesarean deliveries, placenta previa, and chronic urological conditions referred her to a high-risk category. Identifying such risk factors is essential for early diagnosis, appropriate imaging, and planning delivery in specialized centers.</p></sec><sec><title>The classification / Классификация</title><p>The traditional PAS classification used widely for many years is based on assessing the depth of chorionic villi invasion [<xref ref-type="bibr" rid="cit4">4</xref>]:</p><p>The currently accepted PAS classification was proposed by the International Federation of Gynecology and Obstetrics (FIGO), which includes [<xref ref-type="bibr" rid="cit5">5</xref>]:</p><p>The precise PAS etiopathogenesis remains under investigation. One hypothesis links PAS to defective decidual formation (e.g., lacked decidua basalis or underdeveloped fibrinoid layer), abnormal vascular remodeling during pregnancy, and excessive trophoblastic invasion, particularly following prior uterine surgery.</p><p>Placental adherence may be:</p><p>Over the past four decades, cesarean section rates have risen by over 20 %, while PAS cases have increased tenfold [<xref ref-type="bibr" rid="cit6">6</xref>]. The prevalence of PAS varies between 1 in 500 to 1 in 10,000 deliveries, with complete placental invasion being particularly rare – around 1 in 24,506 births [<xref ref-type="bibr" rid="cit7">7</xref>][<xref ref-type="bibr" rid="cit8">8</xref>]. Among PAS cases: accreta accounts for 60–75 %, increta for 15–20 %, and percreta for 5–10 %.</p></sec><sec><title>Diagnostic challenges and controversies / Проблемы диагностики и спорные вопросы</title><p>Despite ultrasound being the primary tool for PAS detection, distinguishing between placenta accreta, increta, and percreta remains challenging using grayscale imaging alone. Depth of invasion is difficult to assess due to overlapping sonographic features and variation in interpretation. Classic markers such as placental lacunae, myometrial thinning, and loss of the retroplacental clear zone are helpful but not specific, especially in early gestation.</p><p>Color Doppler imaging and emerging signs such as the “rail sign” (vascular bridging between placenta and adjacent tissues) improve diagnostic precision. However, these findings are not yet standardized and require operator experience and high-resolution equipment. Likewise, advanced tools like 3D power Doppler and shear-wave elastography are being explored but are not yet widely adopted into routine clinical protocols. Unlike most previously reported cases, current report highlights the diagnostic contribution of the "rail sign" on color Doppler as an early marker of placenta increta, verified later by MRI. To our knowledge, such a detailed correlation between Doppler vascular markers and intraoperative findings has been rarely documented.</p><p>The present case contributes to this field by demonstrating the practical value of vascular Doppler markers for diagnosing placenta increta and early signs of PAS 3a.</p></sec><sec><title>Developing diagnostics / Развитие диагностики</title><p>Historically, PAS was only diagnosed postnatally upon complicated placental separation or postpartum hemorrhage, as seen in early reports by Forster, Irving, and Hertig. Today, ultrasound is the primary modality for antenatal detection [9–12].</p><p>The meta-analysis by D’Antonio et al. assessing 3,070 high-risk pregnancies, demonstrated that ultrasound sensitivity and specificity comprised 90.72 % and 96.94 %, respectively, for PAS diagnosis [<xref ref-type="bibr" rid="cit13">13</xref>].</p><p>Sonographic indicators of PAS include [<xref ref-type="bibr" rid="cit14">14</xref>][<xref ref-type="bibr" rid="cit15">15</xref>]:</p><p>Key Doppler criteria include [<xref ref-type="bibr" rid="cit10">10</xref>][<xref ref-type="bibr" rid="cit11">11</xref>]:</p><p>Early diagnosis allows for planned delivery in tertiary centers, reduces emergency hysterectomy rates, and improves maternal and neonatal outcomes. While cases of antenatal PAS diagnosis are well-documented globally, such reports are limited in Georgian literature. This article presents a clinical case that illustrates the role of modern ultrasound, particularly Doppler techniques, in the diagnosis and management of placenta increta.</p></sec><sec><title>Case presentation / Клинический случай</title><p>Patient D., 29 years old, has a history of three cesarean deliveries (in 2014, 2017, and 2025). The somatic history is significant for chronic pyelonephritis and urolithiasis.</p><p>The patient underwent routine screening examinations at 8, 12, 20, 23, and 28⁺⁶ weeks of gestation. Standard transvaginal and transabdominal ultrasounds were performed. After diagnosing placenta increta, magnetic resonance imaging (MRI) was additionally conducted. The diagnosis was confirmed intraoperatively and by histopathological examination.</p><p>At gestational age of 8 weeks, first-degree invasion of the gestational sac into the scar area was observed.</p><p>At 12–13 weeks of gestation, the placenta was localized on the anterior uterine wall, in the lower segment, covering the medial aspect of the postoperative scar and extending to the internal os of the endocervical canal – indicating placenta previa (Fig. 1).</p><fig id="fig-1"><caption><p>Figure 1. Patient D. at 12–13 weeks of pregnancy.</p><p>Рисунок 1. Пациентка Д. на 12–13‑й неделе беременности.</p></caption><graphic xlink:href="akusherstvo-20-1-g001.jpeg"><uri content-type="original_file">https://cdn.elpub.ru/assets/journals/akusherstvo/2026/1/hTojjJVXLW7RHcFSlkY3HKvtVsqmWL8x1l9Uiaw7.jpeg</uri></graphic></fig><p>During the 12-week screening, both placenta previa and partial invasion into the residual myometrium were identified. The patient was classified as high-risk for placental implantation anomalies and was informed about potential complications (Fig. 2).</p><fig id="fig-2"><caption><p>Figure 2. Patient D. at 15–16 weeks of pregnancy.</p><p>Рисунок 2. Пациентка Д. на 15–16‑й неделе беременности.</p></caption><graphic xlink:href="akusherstvo-20-1-g002.jpeg"><uri content-type="original_file">https://cdn.elpub.ru/assets/journals/akusherstvo/2026/1/HEmtWJ2X9kepcsidXi4QnShdJZzGV17E5Us1Knbm.jpeg</uri></graphic></fig><p>At 19 weeks of gestation, the ultrasound revealed placenta previa localized over the anterior uterine wall at the site of the previous cesarean scar. The myometrial thickness over the scar was 3.2 mm, indicating its significant thinning. Multiple irregular placental lacunae, ranging in size from 4 to 10 mm, were observed with chaotic flow patterns (Fig. 3). Color Doppler examination showed hypervascularity in the retroplacental and bladder interface zone. Peak systolic velocities exceeded 20 cm/s, with low-resistance arterial and venous flow consistent with abnormally invasive vasculature (Fig. 4).</p><fig id="fig-3"><caption><p>Figure 3. Patient D., 20 weeks of pregnancy.</p><p>Рисунок 3. Пациентка Д., 20 недель беременности.</p></caption><graphic xlink:href="akusherstvo-20-1-g003.jpeg"><uri content-type="original_file">https://cdn.elpub.ru/assets/journals/akusherstvo/2026/1/1XUPKsIhhc0bcfAdUrzJ9Uhdj2TVOz5mOgwb0vaV.jpeg</uri></graphic></fig><fig id="fig-4"><caption><p>Figure 4. Patient D., 24 weeks of pregnancy.</p><p>Рисунок 4. Пациентка Д., 24 недели беременности.</p></caption><graphic xlink:href="akusherstvo-20-1-g004.jpeg"><uri content-type="original_file">https://cdn.elpub.ru/assets/journals/akusherstvo/2026/1/scz6YNLINqoXoXjwgWKWtVJPe7BPpVirUPL7xkDM.jpeg</uri></graphic></fig><p>By 28⁺⁶ weeks of gestational age, placental bulging and invasion into the cervical canal were documented, consistent with PAS 3a. The Doppler “rail sign,” characterized by parallel bridging vessels extending from the myometrium through the serosa, was clearly visualized.</p><p>At 24 weeks of gestation, placenta previa was noted again. The myometrial structure could not be assessed as the placenta was fully invading it; the serosal layer remained intact, the endocervical canal was closed, with its length was 40 mm. According to the FIGO classification, this corresponded to PAS 2.</p><p>At 28⁺⁶ weeks of gestational age, transvaginal scanning revealed invasion of the placenta into the upper third of the cervix and the cervical canal corresponding to PAS 3a (Table 1).</p><table-wrap id="table-1"><caption><p>Table 1. Timeline summary of ultrasound and Doppler parameters in placenta accreta spectrum (PAS) diagnosis.</p><p>Таблица 1. Хронология ультразвуковых и доплеровских параметров при диагностике placenta accreta spectrum (PAS).</p></caption><table><tbody><tr><td>Gestational age
Гестационный возраст</td><td>Findings
Результаты</td><td>Myometrial thickness
Толщина миометрия</td><td>Lacunae
Лакуны</td><td>Doppler velocity
Доплеровская скорость</td><td>PAS classification
Классификация PAS</td></tr><tr><td>8 weeks
8 недель</td><td>Suspected scar invasion
Подозрение на инвазию в рубец</td><td>Not measurable
Неизмеримо</td><td>Not present
Отсутствуют</td><td>Not assessed
Не оценивалась</td><td>–</td></tr><tr><td>12 weeks
12 недель</td><td>Partial intra-scar invasion
Частичная инвазия в рубец</td><td>~4 mm
~4 мм</td><td>Small lacunae
Небольшие лакуны</td><td>Mild flow
Слабое течение</td><td>Suspected PAS 1–2
Подозрение на PAS 1–2</td></tr><tr><td>19 weeks
19 недель</td><td>Placenta previa, hypervascularity
Предлежание плаценты, гиперваскуляризация</td><td>3.2 mm
3,2 мм</td><td>Multiple (4–10 mm)
Множественные (4–10 мм)</td><td>&gt; 20 cm/s
&gt; 20 cм/с</td><td>PAS 2
PAS 2</td></tr><tr><td>28⁺⁶ weeks
28⁺⁶ недель</td><td>Cervical invasion, “rail sign”
Инвазия в шейку матки, «рельсовый симптом»</td><td>Thinned, indistinct
Истонченный, нечеткий</td><td>Enlarged lacunae
Увеличенные лакуны</td><td>Persistent turbulent flow
Постоянное турбулентное течение</td><td>PAS 3a
PAS 3а</td></tr></tbody></table></table-wrap><p>Additional Doppler imaging allowed to identify vascular bridges (rail sign) extending from the myometrium through the serosal layer, defined as placenta increta (PAS 2).</p><p>Subsequent MRI confirmed complete placenta previa, with abnormal growth into the uterine scar and across all layers of the myometrium.</p><p>Doppler evaluation of blood flow proved to be a valuable tool for assessing the degree of abnormal placental invasion.</p><p>This clinical case demonstrates the effectiveness of modern ultrasonographic technologies, particularly color Doppler imaging, in diagnosing deep placental invasion. Although Jauniaux et al. previously emphasized the limitations for ultrasound in assessing the depth of placenta increta, this case challenges that viewpoint [<xref ref-type="bibr" rid="cit16">16</xref>].</p><p>The MRI findings corroborated the Doppler-based suspicion of placenta increta with cervical extension (PAS 3a), confirming the depth of myometrial invasion and its relationship to adjacent structures [<xref ref-type="bibr" rid="cit17">17</xref>]. The diagnostic features, such as myometrial thinning, enlarged lacunae, and abnormal vascular bridging (“rail sign”), are consistent with the FIGO classification for PAS and align with Jauniaux et al.’s standardized ultrasound descriptors. Furthermore, the approach is consistent with the Society for Maternal-Fetal Medicine (SMFM) recommendations, which emphasize the use of grayscale and Doppler imaging for antenatal diagnosis and risk stratification.</p><p>While the FIGO classification provides a standardized framework for defining PAS disorders, it has notable limitations. Several specialists have argued that its reliance on histopathological criteria offers little value intraoperatively, when real-time surgical decisions are required. Moreover, studies have highlighted that the FIGO grading does not correlate consistently with maternal morbidity, which limits its prognostic utility. In clinical practice, classifications based on surgical and imaging findings, such as those proposed by Jauniaux et al. (2019) or SMFM, may be more useful, as they emphasize parameters that directly influence management planning, surgical complexity, and outcomes [<xref ref-type="bibr" rid="cit18">18</xref>]. Incorporating these clinically oriented frameworks alongside FIGO may therefore provide a more comprehensive approach for risk stratification and operative preparation.</p><p>We recognize that antenatal ultrasound PAS diagnosis has been well established in the literature. However, the presented case adds more value by demonstrating the utility of the "rail sign" in early gestation and confirming its correlation with MRI and histopathology, thereby reinforcing the clinical applicability of this marker in routine practice.</p><p>An additional limitation relates to the pathological assessment per se. Histopathological confirmation is traditionally regarded as the gold standard for PAS diagnosis; however, its validity has been questioned. The degree of placental adherence can vary even within the same specimen, and a diagnosis of placenta increta or percreta may be influenced by the site from which tissue is sampled. This introduces the risk of sampling bias and may lead to under- or over-classification of PAS severity. For this reason, intraoperative findings and the overall clinical context should be considered alongside histological results while establishing a definitive diagnosis.</p><p>Despite its high sensitivity and specificity, ultrasound (even when combined with color Doppler or MRI) cannot fully predict the intraoperative degree of surgical difficulty. Numerous studies have shown discrepancies between antenatal imaging findings and actual operative challenges, particularly regarding the extent of vascular invasion, adhesion severity, and risk of hemorrhage. Therefore, while imaging plays a critical role in early detection and management planning, it should not be overestimated as a predictor of surgical complexity. Multidisciplinary readiness and intraoperative adaptability remain essential in managing PAS cases.</p><p>Early detection of PAS, especially placenta percreta variants, is vital for maternal and fetal survival, allowing for planned surgical management in high-resource settings. This case illustrates how the integration of Doppler markers into standard prenatal surveillance can improve outcomes and reduce a need for emergency interventions. While limited to a single patient, the findings presented contribute to the growing body of evidence supporting the role for advanced ultrasound in PAS diagnosis. Further studies are needed to validate these vascular markers across diverse clinical settings.</p></sec><sec><title>Conclusion / Заключение</title><p>Over the past four decades, the rise in placenta accreta cases has underscored the urgent need for timely and accurate diagnosis of this high-risk pregnancy complication. The growing prevalence of PAS disorders parallels the global increase in cesarean deliveries. Current classification systems, such as the FIGO framework, have facilitated systematic diagnosis and clinical management of PAS variants.</p><p>This clinical case reinforces the value of ultrasound, including transvaginal scanning and Doppler imaging, as effective, accessible tools for evaluating the depth of placental invasion. Notably, the use of Doppler-based vascular signs, such as the “rail sign,” provided early indicators of placenta increta with cervical extension (PAS 3a), which were later verified by MRI. This case illustrates how the integration of advanced ultrasound technologies can markedly enhance diagnostic accuracy.</p><p>Early PAS identification allows for planned delivery in specialized centers, reducing maternal morbidity and emergency surgical interventions. The presented case underscores how incorporating Doppler markers into routine screening of high-risk patients can influence clinical decision-making, including the timing of delivery, surgical preparation, and maternal outcome optimization. Continuous ultrasonographic monitoring in high-risk pregnancies and incorporation of novel imaging markers into routine protocols may improve perinatal outcomes and guide future PAS management strategies.</p><p>While based on a single case, these findings highlight the promise of combining Doppler sonography with anatomical imaging, supporting future research into diagnostic standardization and validation.</p></sec></body><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Irving C., Hertig A.T. A study of placenta accreta. Surg Gynecol Obstet. 1937;64:178–200.</mixed-citation><mixed-citation xml:lang="en">Irving C., Hertig A.T. A study of placenta accreta. 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