Preoperative Giant Sacrococcygeal Teratoma Embolization in a Newborn – a Case Report and a Review

Total Page:16

File Type:pdf, Size:1020Kb

Preoperative Giant Sacrococcygeal Teratoma Embolization in a Newborn – a Case Report and a Review Clinical Case Cir Pediatr. 2020; 33: 95-98 Preoperative giant sacrococcygeal teratoma embolization in a newborn – A case report and a review J. Guitart, M. Teixidor, N. Brun, S. López, E. Criado, N. Romero Parc Taulí Healthcare and University Corporation. Sabadell, Barcelona (Spain). Abstract La embolización selectiva antes de la cirugía de resección del Sacrococcygeal teratoma (SCT) is the most frequent congenital TSC gigante es factible y aparece como una técnica segura y útil en germ cell tumor. Patients have a higher risk of perinatal complica- el control del sangrado perioperatorio. tions and death, with bleeding and cardiac decompensation being the most common causes of neonatal mortality. Palabras Clave: Teratoma sacrococcígeo; Recién nacido pre- This is the case of a 35-week preterm newborn with a large SCT maturo; Embolización; Arteria sacra media; Embolización prequi- diagnosed at ultrasound screening in the second trimester. Preop- rúrgica. erative selective embolization of the middle sacral artery and total surgical resection were performed postnatally with minimal blood loss. The patient was discharged at 25 days of life with a normal physical examination. INTRODUCTION Selective embolization prior to giant SCT resection is feasible and appears as a safe and useful technique in the control of periop- Sacrococcygeal teratoma (SCT) is the most frequent erative bleeding. germ cell tumor in pediatric age and the most common (1) Key Words: Sacrococcygeal teratoma; Preterm newborn; Embo- perceptible fetal neoplasia . Typically, it is diagnosed at lization; Middle sacral artery; Preoperative embolization. prenatal control ultrasound screening as an intrauterine mass. Lesions over 10 cm are associated with high perinatal mortality, especially if they are hypervascular, if they have Embolización preoperatoria de teratoma been caused by intraoperative bleeding, or if they are com- sacrococcígeo gigante en un recién nacido. plications arising from congestive cardiac insufficiency. Reporte de un caso y revisión These tumors are usually irrigated by a hypertrophic middle Resumen sacral artery, so arterial ligation or control are a key step in El teratoma sacrococcígeo (TSC) es el tumor congénito de cé- the surgical procedure. A comprehensive literature search lulas germinales más frecuente. Los pacientes afectados tienen un showed three preoperative SCT embolization cases only(2-4). mayor riesgo de complicaciones perinatales y muerte, siendo la This is the case of a patient born at 35 weeks gestation with hemorragia y la descompensación cardiaca las causas más comunes type 1 giant SCT successfully embolized prior to surgical de mortalidad neonatal. removal. The objective of this article was to describe the Presentamos el caso de un recién nacido pretérmino de 35 se- endovascular procedure and discuss benefits and risks. manas con un TSC de gran tamaño diagnosticado por ecografía en el segundo trimestre. La embolización selectiva preoperatoria de la arteria sacra media y la resección quirúrgica total postnatal se realizaron con una mínima pérdida de sangre. El paciente fue dado CINICAL CASE de alta a los 25 días de vida con un examen físico normal. Preterm 35-week newborn diagnosed with giant SCT prenatally. Ultrasound screening in the second trimester and subsequent fetal MRI at 29 weeks gestation confirmed the presence of a type 1 SCT according to Altman’s clas- Corresponding author: Dr. Josep Guitart Giménez. Parc del Taulí, 1. 08208 sification. No signs of cardiac insufficiency were noted Sabadell, Barcelona (Spain). at subsequent fetal echocardiograms. An urgent cesarean E-mail address: [email protected] section was carried out as a result of a premature rupture Date of submission: October 2019 Date of acceptance: January 2020 of the membranes and anomalies in the associated cardio- VOL. 33 No. 2, 2020 Preoperative giant sacrococcygeal teratoma embolization in a newborn – A case report and a review 95 Figure 1. Middle sacral artery hypertrophy (arrow tips) with signif- Figure 2. Aortoiliac angiogram following embolization with Gel- icant neovascularization in the tumor bed. foam® and microcoils. tion through the middle sacral artery, decision was made to try preoperative embolization under general anesthesia 18 hours following delivery. Given that the common femoral artery approach was not feasible due to the position of the patient’s limbs – as a result of the tumor’s size –, the left common carotid artery (CCA) was used following surgical exposure. An abdominal aortography was performed by means of a manual contrast injection using a 4F vascular introducer sheath and a 4F multipurpose catheter. 250 IU of heparin were adminis- tered through the introducer sheath. Lower abdominal aorta angiogram demonstrated the presence of a large hypervascu- larized mass irrigated by a significantly hypertrophic mid- dle sacral artery (Fig. 1) and, to a lesser extent, by some lateral sacral branches of the left hypogastric artery. The Figure 3. Tumor appearance prior to the procedure (18 hours following embolization) showing signs of ischemia and necrosis. middle sacral artery was selectively catheterized using a 2.7F microcatheter (Progreat®, Terumo Europe) and suc- cessfully embolized with Gelfoam® (Pfizer, Spain) and two proximal pushable microcoils (Fig. 2). Embolization was tocographic record. Patient weight at birth, including the performed with 5 ml of iodinated contrast diluted in 10 ml of tumor, was 4,030 g. SCT was approximately 19 x 15 cm in saline solution. Total procedure time, including the surgical size and had ulcerations and bleeding signs on its surface. dissection of the left CCA, was 90 minutes. The patient was An echocardiogram was performed at 24 hours of life. moved to the neonatal ICU without further complications. It demonstrated a 3 mm persistent ductus arteriousus with The elective procedure was carried out the following day, left-right communication – which was normal considering at 38 hours of life, through a posterior sacral access, with the hours since birth – and no further relevant disorders a minor intraoperative blood loss that required a 5 ml/kg (73% ejection fraction). red blood cell concentrate transfusion, and with a 9.8 g/dl Owing to ulcerations and size, elective surgical removal final hemoglobin level. Prior to removal, the tumor had a at 24 hours was indicated. In order to control tumor irriga- purplish ischemic appearance with necrotic areas (Fig. 3). 96 J. Guitart et al. CIRUGÍA PEDIÁTRICA The tumor’s pathological anatomy confirmed diagno- resents nearly 70% of general mortality in the neonatal sis of immature congenital teratoma (with a maximum period. To prevent this risk, an adequate surgical dissec- diameter of 18 cm) and fragment of coccyx with adjacent tion should be carried out. Early occlusion of the arteries teratomatous elements (pancreatic tissue). The patient irrigating the tumor can also prove useful. was discharged at 25 days of life with a normal physical The middle sacral artery usually irrigates the SCT, and examination. can be as hypertrophic as the common iliac artery, which may cause vascular steal syndrome(10). The tumor can also be irrigated by both internal iliac artery branches, primarily DISCUSSION through the lateral sacral arteries. There are few cases published in the literature describ- This is the case of a successful preoperative SCT ing tumor devascularization prior to tumor removal by embolization using a left common carotid artery (CCA) ligating the middle sacral artery or the internal iliac arter- approach. CCA access, either through arteriotomy, or more ies, or by performing a temporal clamping of the abdominal recently, through percutaneous access(5), has already been aorta(11). described in infants with congenital cardiopathy undergo- To our knowledge, there are only 3 cases published ing cardiac catheterization. However, there is little infor- where preoperative hemostatic control was carried out mation on its use for other vascular procedures. To our using an endovascular approach. knowledge, there are only 3 SCT cases published where In 2006, Cowles et al. published the case of a 36-week preoperative hemostatic control was carried out using newborn with a large type 1 SCT undergoing arterial embo- an endovascular approach, and only 1(3) where the CCA lization and subsequent direct radiofrequency percutaneous approach was used. ablation for hemostatic control purposes prior to surgical Prenatally diagnosed SCT is difficult to manage as it resection. In this patient, the vascular access was carried is highly unpredictable. Perinatal mortality ranges from out through the right common femoral artery. The mid- 40% to 50%(6). dle sacral artery, the lateral sacral arteries, and the gluteal Imaging characteristics, particularly >10 cm tumor vol- artery were embolized using Gelfoam® and acrylic glue(2). ume, and associated with solid component, can provide In 2011 and 2013, respectively, Lahdes-Vasama et al.(3) prognostic information(6). Other factors associated with and Rossi et al.(4) described the preoperative devascular- high risk SCT include polyhydramnios and rapid tumor ization of a giant SCT using an endovascular approach growth. Fetal cardiac dysfunction (often associated with only. In the first case, the patient was a 30-week preterm non-immune hydrops), spontaneous tumor bleeding, and newborn; and similarly to our case, common carotid artery preterm delivery are also highly associated with perinatal access was decided upon. mortality and morbidity(7).
Recommended publications
  • From Sacrum to Spine: a Complex Case of Sacrococcygeal Teratoma
    From Sacrum to Spine: A Complex Case of Sacrococcygeal Teratoma Jennifer Young, MN, RN(EC) NP-Pediatrics, NNP-BC Hazel Pleasants-Terashita, MN, RN(EC) NP-Pediatrics, NNP-BC Continuing Nursing Education (CNE) ABSTRACT Credit The test questions are pro- Neonatal tumors occur infrequently; sacrococcygeal teratoma (SCT) is a rare and abnormal mass vided in this issue. The often diagnosed on antenatal ultrasound. An SCT may cause serious antenatal complications, requires posttest and evaluation must be com- surgery in the neonatal period, and can lead to various long-term sequelae including fecal incontinence pleted online. Details to complete the course are provided online at acade- or constipation, urinary incontinence, and lower extremity mobility impairment. Even rarer are SCTs myonline.org. Sign into your ANN that include intraspinal extension necessitating complex neurosurgical intervention to relieve possible account or register for a non-member spinal cord compression or tumor tissue resection. A comprehensive understanding of the natural account if you are not a member. A total of 1.5 contact hour(s) can be earned as history of SCT provides frontline neonatal nurses and nurse practitioners with the expertise and CNE credit for reading this article, language to support families during an infant’s NICU admission. A glossary of key terms accompanied studying the content, and completing the online posttest and evaluation. To by a case review of a premature infant born with a large external SCT with intrapelvic and intraspinal be successful, the learner must obtain a components aids in enhancing knowledge related to the potential impact of an SCT on the central grade of at least 80 percent on the test.
    [Show full text]
  • Sacrococcygeal Teratoma and Normal Alphafetoprotein Concentration on September 26, 2021 by Guest
    J Med Genet: first published as 10.1136/jmg.22.5.405 on 1 October 1985. Downloaded from Case reports 405 Lymphocyte studies revealed the mother's band has been incorporated into another breakpoint chromosomes to be normal. The father was unavail- site. The smallness of the deleted segment may able for study. explain her minimal dysmorphogenetic features; however, there is a lack of clinical similarity Discussion between our patient and the other two cases of interstitial 2p deletions. For example, our patient The clinical features of patients with deletions of 2p had premature closure of her fontanelles, whereas are summarised in the table. The patient of three other patients, including one with a deleted Ferguson-Smith et at2 is not included in the tabula- segment incorporating band 2p14,4 had delayed tion because he was also partially trisomic for the closure of their fontanelles. It is possible that our distal four bands of Sq and so was not a pure case of patient's physical and mental stigmata are the partial 2p monosomy. The patient reported by consequence of a disruption in one or more gene's Zachai et at5 is identical to case 2 of Emanuel et al. 1 nucleotide sequence resulting from this child's Given the paucity of reported cases, only the most numerous chromosome breaks. Given the uncer- tentative statements can be made regarding the tainty of our patient's karyotype and the limited clinical picture associated with deletions of 2p. The number of 2p deletion cases, it is evident that more Iwo cases presented by Emanuel et all have nearly cases of 2p deletions are required before a clear cut identical deleted segments and share the following 2p deletion syndrome, or syndromes, emerges.
    [Show full text]
  • Cancer Research and Reports an Open Access Journal CRR-1-E102
    Cancer Research and Reports An open access journal CRR-1-e102 Editorial Paediatric Gynaecologic Neoplasms Abdelrahman K Hanafy, Priya R Bhosale, Ajaykumar C Morani* Departments of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA Introduction common than mature teratomas. Degree of malignancy is determined based on the level of neuroectodermal component A variety of gynaecologic neoplasms occur in the pediatric differentiation in tissue samples [11]. Teratomas can also occur population. Differentiating between benign and malignant extragonadal; the important one which needs a particular lesions and reaching the correct diagnosis in a timely manner is mention includes sacrococcygeal teratoma (SCT). SCT is the crucial to preserve fertility, which is a priority in this most common teratoma in neonates, and often detected on population. Awareness of the clinical, laboratory and pertinent prenatal US. Most SCTs are benign at birth; however, imaging characteristics of such lesions will facilitate their malignant transformation can occur. Associated anorectal and recognition in clinical practice. genitourinary malformations may also occur. MRI is the best modality for depicting this lesion and evaluating surrounding Ovarian neoplasms structures for invasion. After resection of SCT, surveillance for recurrence is recommended for 3 years utilizing a combination Ovarian tumors are uncommon in childhood having an of physical exam, AFP levels and periodic pelvic imaging [12- incidence of 2.6 /100,000 girls per year. Majority of these are 14]. Dysgerminoma is the most common malignant ovarian benign; less than one third are malignant [1,2]. Presentation is germ cell tumor (MOGCT). On MRI, it appears as a solid usually as a palpable mass or abdominal pain.
    [Show full text]
  • ULTRASOUND STUDY GUIDE • Technical Knowledge O Physics And
    ULTRASOUND STUDY GUIDE Technical knowledge o Physics and Safety, understand the following: 1) Physics of sound interactions in the body. 2) How transducers work, how the image is created, and what physical properties are being displayed. 3) Relative strengths and weaknesses of different transducers including various aspects of resolution. Sound properties and interactions Reflection Attenuation Scattering Refraction Absorption Acoustic impedance Speed of sound Wavelength Other . Transducer fundamentals Transmit frequencies Transducer components Transducer types Transducer pros and cons Other . Beam formation Focusing Steering Other . Imaging modes and display 2D 3D 4D Panoramic imaging Compound imaging Harmonic imaging Elastography Contrast imaging Scanning modes o 2D o 3D o 4D o M-mode o Doppler o Other Image orientation Other . Image resolution Axial Lateral Elevational / Azimuthal Temporal Contrast Penetration vs. resolution Other . System Controls - Know the function of the controls listed below and be able to recognize them in the list of scan parameters shown on the image monitor Gain Time gain compensation Power output Focal zone Transmit frequency Depth Width Zoom / Magnification Dynamic range Frame rate Line density Frame averaging / persistence Other . Doppler / Flow imaging – Be familiar with the terminology used to describe Doppler exams. Be able to interpret and optimize the images. Be able to recognize artifacts, know their significance, and know what produces them. Doppler
    [Show full text]
  • Sacrococcygeal Teratoma in the Perinatal Period
    754 Postgrad Med J 2000;76:754–759 Postgrad Med J: first published as 10.1136/pgmj.76.902.754 on 1 December 2000. Downloaded from Sacrococcygeal teratoma in the perinatal period R Tuladhar, S K Patole, J S Whitehall Teratomas are formed when germ cell tumours tissues are less commonly identified.12 An ocu- arise from the embryonal compartment. The lar lens present as lentinoids (lens-like cells), as name is derived from the Greek word “teratos” well as a completely formed eye, have been which literally means “monster”. The ending found within sacrococcygeal teratomas.10 11 “-oma” denotes a neoplasm.1 Parizek et al reported a mature teratoma containing the lower half of a human body in Incidence one of fraternal twins.13 Sacrococcygeal teratoma is the most common congenital tumour in the neonate, reported in Size approximately 1/35 000 to 1/40 000 live Size of a sacrococcygeal teratoma (average 8 births.2 Approximately 80% of aVected infants cm, range 1 to 30 cm) does not predict its bio- are female—a 4:1 female to male preponder- logical behaviour.8 Altman et al have defined ance.2 the size of sacrococcygeal teratomas as follows: The first reported case was inscribed on a small, 2 to 5 cm diameter; moderate, 5 to 10 Chaldean cuneiform tablet dated approxi- cm diameter; large, > 10 cm diameter.14 mately 2000 BC.3 In the modern era, the first large series of infants and children with sacro- Site coccygeal teratomas was reported by Gross et The sacrococcygeal region is the most com- al in 1951.4 mon location.
    [Show full text]
  • Obstetrics and Gynecology Practice Analysis Detailed Report
    Obstetrics and Gynecology Practice Analysis Detailed Report ARDMS approved March 2021. CONFIDENTIALITY NOTICE The information contained within this report is confidential and is for the exclusive use for Inteleos. No redistribution or subsequent disclosure of this document is permitted without prior authorization from Inteleos. OB/GYN Practice Analysis Report Contents ACKNOWLEDGEMENTS .............................................................................................................................................. 3 EXECUTIVE SUMMARY ................................................................................................................................................ 4 BACKGROUND OF STUDY .......................................................................................................................................... 4 METHODOLOGY ............................................................................................................................................................ 4 Selection and Profile of Subject Matter Experts ............................................................................................ 4 Workshop Panel .................................................................................................................................................. 4 Remote Panel ...................................................................................................................................................... 4 Panelist Interviews and Workshop ....................................................................................................................
    [Show full text]
  • View Showed Solid Tissue Fragments Composed of Mature Neural Tissue Comprising Glial Cells and Astrocytes with No Other Germ Cell Layer Component
    Saadaat et al. Surgical and Experimental Pathology (2019) 2:24 Surgical and Experimental https://doi.org/10.1186/s42047-019-0049-4 Pathology CASE REPORT Open Access Brain ectopic tissue in sacrococcygeal region of a child, clinically mimicking sacrococcygeal teratoma: a case report Ramin Saadaat1, Jamshid Abdul-Ghafar1*, Ahmed Nasir2, Soma Rahmani2 and Hidayatullah Hamidi2 Abstract Background: Mature brain heterotopic tissue in sacrococcygeal region is a very rare benign congenital abnormality of newborn. To date, only two cases of mature heterotopic brain tissue in the sacrococcygeal region is reported by literature. Heterotopic brain tissue in other areas such as lung, nose, face and retroperitoneal region are also rarely reported. Meanwhile, rather than brain heterotopic tissue in sacrococcygeal region, a case of adrenal gland heterotopic tissue in sacrococcygeal region also has been reported. Case presentation: A 3.5 month-old male baby presented with history of sacrococcygeal mass since birth. Clinical examination of the child was good with no other problem. Sacrococcygeal region revealed an elevated round mass with no discharge. Computed tomography reported a large sacrococcygeal teratoma type-III arising from the sacrococcygeal region extending intra-abdominally to the level of L2 vertebral body. The mass was excised by the impression of sacrococcygeal teratoma (SCT). On gross examination, a gray-white irregular tissue fragment with 5 cm in greatest dimension was examined. Cut sections showed homogenous yellowish white appearance. Histological examination revealed solid fragments composed of mature neural tissue comprising glial cells and astrocytes with no other germ cell layer component. Conclusion: Mature brain heterotopic tissue in sacrococcygeal area is a rare benign disease.
    [Show full text]
  • Sacrococcygeal Teratomateratoma Brock W
    SacrococcygealSacrococcygeal TeratomaTeratoma Brock W. Hanisch Creighton University, Department of Clinical Anatomy Brock W. Hanisch Creighton University, Department of Clinical Anatomy SacrococcygealSacrococcygeal TeratomaTeratoma (SCT)(SCT) •The most common tumor found in newborns. •"Sacro" refers to sacrum and "coccy" refers to coccyx. •Teratoma refers to the type of tissues that make up these growths. They are comprised of chaotically arranged tissues of all types (fat, bone, nerves, muscle, etc…) that are found in an area that they are not normally found. •Sacrococcygeal teratoma (SCT) is rare, occurring in 1 in 35,000 to 40,000 live births. •It is four times more common in females than males. The cause is not known. One theory is it is a failed twinning attempt. Another is it is a growth from an abnormally placed set of germ or stem cells. SacrococcygealSacrococcygeal TeratomaTeratoma (SCT)(SCT) •Those diagnosed in utero carry 50% risk of premature delivery. •Sacrococcygeal teratomas can be quite large. Many are approximately the size of the unborn baby. Tumors greater than 10cm in diameter require cesarean. •Some of the SCTs are cyst-type tumors, meaning they are filled with fluid. Others are solid tumors that may have a significant amount of blood flow through them. The most common type of SCT is a combination of both solid and cystic. •Tumor develops from pluripotential embryonic cells (remnants of primitive streak). Origin of SCT Embryology: •Original germ cells migrating from the yolk sac to the gonad pathway are thought to persist, deviate, differentiate, and mature, typically resting anterior to the future coccyx at Hensen’s node.
    [Show full text]
  • Sacrococcygeal Teratoma in Children: Audit on Clinical Outcomes from A
    26 European Urology Supplements 18 (4), (2019), 1–34 A remnant of the coccyx may lead to local recurrence. However, there GCT-61 Controlled aspiration of large paediatric ovarian is difficult to recognize the transition between coccyx and sacrum. cystic tumours Besides that, the tumour can infiltrate the sacrum and more extensive resection could be necessary. Intraoperative magnetic resonance imaging (MRI) can be used to assist resection of central nervous E. Gavens1, L. Watson1, M. Pachl1, G.S. Arul1 system tumours. We adapted this technique to sacrococcygeal 1Department of Paediatric Surgery, Birmingham Children’s Hospital, tumours. The aim of this study was to discuss the operative technique Birmingham, UK of image guidance with MRI in the surgical management of Background: Aetiology of large ovarian cystic masses in children sacrococcygeal tumours. includes physiological and neoplastic cysts. If radiology is suspicious Methods: Retrospective analyses of the sacrococcygeal germ cell for malignancy, cyst is usually removed via large midline incision to tumour operations that intraoperative MRI was used for, with a two avoid risk of spillage, but is painful with cosmetically-unappealing Tesla magnet with a patient transportation system. incisions for young women. We present our experience of using a Results: There were 5 patients: 3 male and 2 female. Age at procedure minimally-invasive approach first described by Ehrlich [1]. was: 3 days, 4 months, 3 years, 4 years and 4 years. Two procedures Methods: Retrospective review of girls with large ovarian cystic were primary resection (one immature and one mature teratoma), and masses at our centre since 2007. Small pfannenstiel incision three for relapse (one in first year and two in second).
    [Show full text]
  • Marketing Fragment 6 X 10.5.T65
    Cambridge University Press 978-0-521-68563-4 - A Practical Guide to Human Cancer Genetics, Third Edition Shirley Hodgson, William Foulkes, Charis Eng and Eamonn Maher Index More information Index Note: page numbers in italics refer to figures and tables N-acetyltransferase alcohol, laryngeal cancer 29 acetylation 61 Allgrove syndrome 43 activity 118 alpha-1 antitrypsin deficiency, hepatocellular achalasia, oesophageal cancer 43 carcinoma 49 acoustic neuroma alphafetoprotein 214 NF2 235–6 alveolar cell carcinoma 30, 31 see also vestibular schwannoma amine compounds, bladder cancer 118, 119 acromegaly, familial 37 Amsterdam Criteria 203 actinic keratosis 148 androgen-insensitivity states, incomplete 111 acute lymphoblastic leukaemia (ALL) angiomyolipomas 247 classification 233 aniridia, sporadic 112, 113, 114 cytogenetic analysis 123–4 anticipation translocations 168 AML 123 acute myeloid leukaemia (AML) 183–4 leukaemia 122 anticipation 123 APC gene classification 120 mutations 190 Klinefelter syndrome 214 benign 191 Kostman syndrome 215 Gardner syndrome 186 acute myelomonocytic leukaemia 233, 234 Turcot syndrome 251 acute promyelocytic leukaemia 168 polymorphism in colon cancer 60 adenocarcinoma, see renal cell carcinoma APKD1 gene 249–50 adenosine deaminase deficiency 245 arsenic 51, 147 adrenal gland tumours asbestos 30 adrenocortical adenoma/carcinoma astrocytoma 13–14 39–40 ataxia telangiectasia 167–9 phaeochromocytoma 37–9 breast cancer 168 adrenocortical hyperplasia 40 gastric adenocarcinoma 46 aflatoxin 48, 51 locus 168 Aicardi syndrome
    [Show full text]
  • Sacrococcygeal Teratoma Excision: a Vertical Rather Than Transverse Wound Closure Amr A
    Original article 207 Sacrococcygeal teratoma excision: a vertical rather than transverse wound closure Amr A. AbouZeid, Mohamed H. Mohamed, Mohamed M. Dahab, Mohamed A. GadAllah and Ahmed M. Zaki Background The chevron incision has been the standard dissection; meanwhile, it provided a well-recognized approach for sacrococcygeal teratoma (SCT) excision. Here, cosmetic advantage. we are reporting our experience of shifting to the vertical Conclusion The vertical posterior sagittal approach for posterior sagittal approach. excision of SCT is both feasible and advantageous in terms Patients and methods During the period 2011 through of the cosmetic outcome. It provides a well-hidden scar in 2016, we operated on 17 (16 female and one male) cases of the natal cleft and preserves normal contouring of the – SCT. Their age at presentation ranged from day 1 to buttocks. Ann Pediatr Surg 13:207 212 c 2017 Annals of 26 months (mean = 4.8 months, median = 2 months). The Pediatric Surgery. chevron incision was used in five, whereas the vertical Annals of Pediatric Surgery 2017, 13:207–212 posterior sagittal approach was used in 12 patients. Keywords: buttock, cosmesis, posterior sagittal, reconstruction, sacrococcygeal teratoma Results In this series, we had one case of perioperative Department of Pediatric Surgery, Faculty of Medicine, Ain-Shams University, mortality, in addition to another case of perineal wound Cairo, Egypt disruption (in the group of vertical wound closure), which Correspondence to Amr A. AbouZeid, MD, Lotefy El-Sayed Street, 9 Ain-Shams was managed conservatively (to heal by secondary University Buildings, Abbassia, Cairo 11657, Eygpt intention) with a very satisfactory hidden scar at 6-month Tel: + 20 111 656 0566; fax: + 20 224 830 833; follow-up.
    [Show full text]
  • Prenatal Diagnosis and Management of Sacrococcygeal
    Obstetrics & Gynecology International Journal Review Article Open Access Review article: prenatal diagnosis and management of sacrococcygeal teratoma, a review of literature Introduction Volume 10 Issue 1 - 2019 A tumor formed from different tissues derived from the 3 germ Mahmoud Alalfy,1 Alaa Elebrashy,2 Osama cell layers away from anatomic place in which it develops. With Azmy,3 Ahmed Elgazzar,4 Ahmed Zakaria,4 advancement in ultrasound, more sacrococcygeal teratomas (SCT) Hassan Gaafar,5 Sameh Hussen,6 Amr are now diagnosed prenatally.1 Abbassy,1 Seif eleslam,7 Hatem Hassan,1 Ebrahem Magdi,8 Adel Husney,8 Mohamed It usually develops near coccyx, where the greatest amount of Hasanen,8 Mahmoud Karoura,8 Sherif primitive cells is present for a long time. Abdalmordy,8 Ahmed Kotby,8 Mohamed Ezz,9 Prevalence: Most common tumor of the newborn, with a prevalence Wael El Guindi10 of 0.25-0.28:10,000 live births. 1Lecturer(Researcher) of Obstetrics and Gynecology, Head of the Fetal medicine unit, Reproductive Health and Family Etiology: Arises from pleuripotent cells of Hensen”s node that is planning department, National Research Centre, Egypt, present anterior to coccyx. Consultant Ob/Gyn, Aljazeerah Hospital, Egypt 2Professor of Obstetrics and Gynecology, Cairo University, Pathogenesis: pleuripotent cell line escapes from control of Egypt 3 embryonic inducers and organizers and differentiates into tissues Professor of Obstetrics and Gynecology, Reproductive Health and Family planning department, National Research Centre, that is not usually present in the sacrococcygeal area. The teratomas Egypt develop and mature during intrauterine life, and get a growth that 4Professor, Obstetrics and Gynecology, Cairo University, Egypt mnatches fetal growth.2 5Assistant professor Obstetrics and Gynecology, Cairo University, Egypt Associated anomalies: There is no specific abnormality that is 6Assistant professor, Reproductive health and family planning more commonly present in sacrococcygeal teratomas than others.
    [Show full text]