Meconium Peritonitis by Segmental Volvulus of the Ileum, Prenatal Diagnosis: Clinical Finding and Literature Review
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Meconium Peritonitis
ISSN: 2377-9004 Agrawal et al. Obstet Gynecol Cases Rev 2020, 7:180 DOI: 10.23937/2377-9004/1410180 Volume 6 | Issue 5 Obstetrics and Open Access Gynaecology Cases - Reviews CASE REPORT Meconium Peritonitis: In Utero Diagnosis of a Rare Clinical Entity and Postnatal Outcome Sarita Agrawal, MD, FICOG, FIAMS, FCGP1, Arpana Verma, MS2*, Sarita Rajbhar, MS3, Pushpawati Thakur, MD4, Loukya Kodumuri, MBBS5 and Swati Kumari, MS, FNB6 1Professor and Head of Department, Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Raipur, Chhattisgarh, India 2Senior Resident, Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Raipur, Chhattisgarh, India 3Assistant Professor, Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Raipur, Chhattisgarh, India 4 Check for Associate Professor, Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, updates Raipur, Chhattisgarh, India 5Post Graduate Student, Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Raipur, Chhattisgarh, India 6Sonologist and Fetal Medicine Expert, Shivam Fetomed and Spine Centre, Raipur, Chhattisgarh, India *Corresponding author: Arpana Verma, MS, Senior Resident, Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, V.V-18, Parthivi Province, Near Salasar Greens, Sarona, Raipur, Chhattisgarh - 492099, India, Tel: 9741412716; 6260334337 Abstract done for immune and non-immune hydrops and was found to be negative. One week later, a repeat ultrasound was done Objective: To present an unusual case of meconium peri- which showed moderate fetal ascites with few areas of calci- tonitis diagnosed during prenatal period and its postnatal fication in the bowel loops and prominent inferior vena cava, outcome. -
Wandering Spleen with Torsion Causing Pancreatic Volvulus and Associated Intrathoracic Gastric Volvulus: an Unusual Triad and Cause of Acute Abdominal Pain
JOP. J Pancreas (Online) 2015 Jan 31; 16(1):78-80. CASE REPORT Wandering Spleen with Torsion Causing Pancreatic Volvulus and Associated Intrathoracic Gastric Volvulus: An Unusual Triad and Cause of Acute Abdominal Pain Yashant Aswani, Karan Manoj Anandpara, Priya Hira Departments of Radiology Seth GS Medical College and KEM Hospital, Mumbai, Maharashtra, India , ABSTRACT Context Wandering spleen is a rare medical entity in which the spleen is orphaned of its usual peritoneal attachments and thus assumes an ever wandering and hypermobile state. This laxity of attachments may even cause torsion of the splenic pedicle. Both gastric volvulus and wandering spleen share a common embryology owing to mal development of the dorsal mesentery. Gastric volvulus complicating a wandering spleen is, however, an extremely unusual association, with a few cases described in literature. Case Report We report a case of a young female who presented with acute abdominal pain and vomiting. Radiological imaging revealed an intrathoracic gastric. Conclusionvolvulus, torsion in an ectopic spleen, and additionally demonstrated a pancreatic volvulus - an unusual triad, reported only once, causing an acute abdomen. The patient subsequently underwent an emergency surgical laparotomy with splenopexy and gastropexy Imaging is a must for definitive diagnosis of wandering spleen and the associated pathologic conditions. Besides, a prompt surgicalINTRODUCTION management circumvents inadvertent outcomes. Laboratory investigations showed the patient to be Wandering spleen, a medical enigma, is a rarity. Even though gastric volvulus and wandering spleen share a anaemic (Hb 9 gm %) with leucocytosis (16,000/cubic common embryological basis; cases of such an mm) and a predominance of polymorphonuclear cells association have rarely been described. -
CASE REPORT CASE CASE R Imaging Findings of Meconium
CASE REPORT CASE REPORT Imaging findings of meconium peritonitis Logeshini Naidoo, MB ChB, FCRad (Diag) SA Helen Joseph and Coronation Hospitals, Johannesburg Introduction Meconium peritonitis results from intrauterine gastrointestinal perfora- tion, and can occur as early as the second trimester.1 Meconium extrudes into the peritoneal cavity, inciting an intense fibroplastic reaction that results in intra-abdominal calcifications.2 It is a rare condition occurring in 1 in 35 000 pregnant women.3 The clinical and radiological manifestations depend on whether the bowel perforation seals off in utero in the neonatal period or remains patent.3 Accordingly, the radiological spectra range from the incidental demonstration of diffuse intra-abdominal calcifications to meconium ascites (free meconium in the peritoneal cavity), meconium pseudocysts (walled-off meconium concentrations), and meconium hydrocoeles. Meconium has also been reported in the thoracic cavity (via diaphrag- matic hernias) and in the pelvic soft tissues.4 Antenatal ultrasound allows early detection of the condition, demonstrating free fluid, hydrocoeles and echogenic foci representing intraperitoneal calcifications.5 In the newborn, plain abdominal radiographs demonstrating calcifications and/or ascites are sufficient for diagnosis.1 Postnatal ultrasound is reserved for atypical presentations and can exclude intra-abdominal masses.1 Although computed tomography (CT) was used as an ancillary tool in the case report described below, it is unnecessary, thus negating the need for radiation exposure and expenditure of time. Fig. 1. Supine abdominal X-ray revealing a massively distended abdomen with poor lung capacities. The bulging flanks and central The imaging findings in a newborn with an ongoing bowel perfora- floating bowel loops indicate ascites. -
Fetal Meconium Peritonitis Associated with Prenatal Methamphetamine Exposure
W.J. Yang, et al ■ SHORT COMMUNICATION ■ FETAL MECONIUM PERITONITIS ASSOCIATED WITH PRENATAL METHAMPHETAMINE EXPOSURE Wen-Jui Yang1, Chie-Pein Chen1,2*, Chen-Yu Chen1, Kuo-Gon Wang1, Tsung-Hsien Su1,2 1Department of Obstetrics and Gynecology, Mackay Memorial Hospital, and 2Mackay Medicine, Nursing and Management College, Taipei, Taiwan. SUMMARY Objective: In roughly 50% of all patients with meconium peritonitis, there is no evidence of primary obstruction of the bowel. We report a case of maternal methamphetamine and heroin abuse complicated by fetal meconium pseudocyst without a definite intestinal obstructive lesion. We discuss the correlation between the presence of meconium peritonitis and prenatal exposure to methamphetamine. Case Report: A 19-year-old, gravida 2, para 0, abortus 1, woman had abused illegal drugs, including methamphetamine and intravenous heroin. Suffering from withdrawal symptoms, she was taken to a shelter where she was diagnosed with a pregnancy of 26 weeks’ gestation. The patient underwent cesarean section at 34 weeks due to preterm labor and fetal malpresentation. A boy weighing 2,474 g was born, but had to be intubated and admitted to the intensive care unit because of a distended abdomen and respiratory distress. A laparotomy performed on the second day of life revealed a large calcified pseudocyst associated with two perforations of the distal jejunum. A segmental resection of the jejunum with primary anastomosis was performed. The infant recovered well after the operation and was discharged 65 days after birth. Conclusion: Since methamphetamine is a powerful _-adrenergic stimulant and induces the release of catecholamines from adrenergic synapses, it can cause powerful vessel constriction. -
Long-Term Outcome After Neonatal Meconium Obstruction
Long-term Outcome After Neonatal Meconium Obstruction Julie R. Fuchs, MD, and Jacob C. Langer, MD ABSTRACT. Objective. It is unclear whether children meconium ileus and those undergoing resection or enter- with cystic fibrosis (CF) who present with neonatal ostomy. Patients with meconium obstruction who do not meconium ileus have a different long-term outcome from have CF have an excellent long-term prognosis. This those presenting later in childhood with pulmonary com- information will be useful in counseling the families of plications or failure to thrive. We examined a cohort of infants presenting with neonatal meconium obstruction. patients with meconium ileus, and compared their long- Pediatrics 1998;101(4). URL: http://www.pediatrics.org/ term outcome with children who had CF without meco- cgi/content/full/101/4/e7; cystic fibrosis, meconium ileus, nium ileus and neonates who had meconium obstruction meconium plug syndrome. without CF (meconium plug syndrome). Study Design. Comparative study using retrospective and follow-up interview data. ABBREVIATION. CF, cystic fibrosis. Patients. Group 1 consisted of 35 surviving CF pa- tients who presented with meconium ileus between 1966 econium obstruction in the neonate is a and 1992. Two control groups were also studied: 35 age- spectrum of disease that includes meco- and sex-matched CF patients without meconium ileus 1 (group 2), and 12 infants presenting with meconium plug Mnium ileus and meconium plug syndrome. syndrome during the same time period (group 3). Meconium ileus is characterized by extremely viscid, Outcome Measures. Pulmonary, gastrointestinal, nu- protein-rich inspissated meconium causing terminal tritional, and functional status were reviewed, and sur- ileal obstruction, and accounts for approximately gical complications were recorded. -
Acute Gastric Volvulus: a Deadly but Commonly Forgotten Complication of Hiatal Hernia Kailee Imperatore Mount Sinai Medical Center
Florida International University FIU Digital Commons All Faculty 3-30-2016 Acute gastric volvulus: a deadly but commonly forgotten complication of hiatal hernia Kailee Imperatore Mount Sinai Medical Center Brandon Olivieri Mount Sinai Medical Center Cristina Vincentelli Mount Sinai Medical Center; Herbert Wertheim College of Medicine, Florida International University, [email protected] Follow this and additional works at: https://digitalcommons.fiu.edu/all_faculty Recommended Citation Imperatore, Kailee; Olivieri, Brandon; and Vincentelli, Cristina, "Acute gastric volvulus: a deadly but commonly forgotten complication of hiatal hernia" (2016). All Faculty. 126. https://digitalcommons.fiu.edu/all_faculty/126 This work is brought to you for free and open access by FIU Digital Commons. It has been accepted for inclusion in All Faculty by an authorized administrator of FIU Digital Commons. For more information, please contact [email protected]. Article / Autopsy Case Report Acute gastric volvulus: a deadly but commonly forgotten complication of hiatal hernia Kailee Imperatorea, Brandon Olivierib, Cristina Vincentellia,c Imperatore K, Olivieri B, Vincentelli C. Acute gastric volvulus: a deadly but commonly forgotten complication of hiatal hernia. Autopsy Case Rep [Internet]. 2016;6(1):21-26. http://dx.doi.org/10.4322/acr.2016.024 ABSTRACT Gastric volvulus is a rare condition resulting from rotation of the stomach beyond 180 degrees. It is a difficult condition to diagnose, mostly because it is rarely considered. Furthermore, the imaging findings are often subtle resulting in many cases being diagnosed at the time of surgery or, as in our case, at autopsy. We present the case of a 76-year-old man with an extensive medical history, including coronary artery disease with multiple bypass grafts, who became diaphoretic and nauseated while eating. -
PROBLEMS of the NEONATAL PERIOD
PROBLEMS of the NEONATAL PERIOD Susan Fisher-Owens, MD, MPH, FAAP Associate Clinical Professor of Clinical Pediatrics Associate Clinical Professor of Preventive and Restorative Dental Sciences University of California, San Francisco Zuckerberg San Francisco General Hospital UCSF Family Medicine Board Review: Improving Clinical Care Across the Lifespan San Francisco March 6, 2017 Disclosures “I have nothing to disclose” (financially) …except appreciation to Colin Partridge, MD, MPH for help with slides 2 Common Neonatal Problems Hypoglycemia Respiratory conditions Infections Polycythemia Bilirubin metabolism/neonatal jaundice Bowel obstruction Birth injuries Rashes Murmurs Feeding difficulties 3 Abbreviations CCAM—congenital cystic adenomatoid malformation CF—cystic fibrosis CMV—cytomegalovirus DFA-- Direct Fluorescent Antibody DOL—days of life ECMO—extracorporeal membrane oxygenation (“bypass”) HFOV– high-flow oxygen ventilation iNO—inhaled nitrous oxide PDA—patent ductus arteriosus4 Hypoglycemia Definition Based on lab Can check a finger stick, but confirm with central level 5 Hypoglycemia Causes Inadequate glycogenolysis cold stress, asphyxia Inadequate glycogen stores prematurity, postdates, intrauterine growth restriction (IUGR), small for gestational age (SGA) Increased glucose consumption asphyxia, sepsis Hyperinsulinism Infant of Diabetic Mother (IDM) 6 Hypoglycemia Treatment Early feeding when possible (breastfeeding, formula, oral glucose) Depending on severity of hypoglycemia and clinical findings, -
Cystic Fibrosis Discussants IVAN HARWOOD, MD; FERNANDO ROSAS, MD; DAVID K
62 im A Cystic Fibrosis Discussants IVAN HARWOOD, MD; FERNANDO ROSAS, MD; DAVID K. EDWARDS, MD; JOHN KELSO, MD; and WILLIAM L. NYHAN, MD, PhD I VAN HARWOOD, MD: * A starting point for the discussion of partial carbon dioxide pressure of 52 torr, and it was decided important topics in cystic fibrosis and its management in to insert an endotracheal tube for ventilation and to begin infants is provided by an informative case of a patient, which treatment with ribavirin. Klebsiella and Escherichia coli will be presented by Dr Rosas. From there we will discuss the were found on tracheal culture. rapidly developing advances in diagnosis and therapy. His course was stormy because of recurrent episodes of increased airway resistance and increased difficulty in ven- Case Presentation tilation, but his condition slowly improved, and the endo- Case 1 tracheal tube was removed about a week later. His weight was FERNANDO RoSAS, MD:t The mother was seen because of 2.3 kg. At 2 months of age, sufficient sweat could be collected polyhydramnios and other factors that led to the decision to for the first time for a sweat test, which was positive; the deliver the infant at 33 weeks by cesarean section. She was 30 chloride concentration was 95.7 mEq per liter and the spec- years old and the father 39. The first offive siblings died at the imen weighed 130 mg. age of 15 months of what was called intestinal infection, the Six weeks after admission, he was discharged weighing fourth was a fetal death at 20 weeks of gestation, and the fifth 2.7 kg and tolerating Pregestimil (Mead Johnson) formula died at 3 months of age of pneumonia. -
Meconium Peritonitis Due to Fetal Appendiceal
Wang et al. BMC Pediatrics (2018) 18:162 https://doi.org/10.1186/s12887-018-1133-8 CASEREPORT Open Access Meconium peritonitis due to fetal appendiceal perforation: two case reports and a brief review of the literature Yi Wang1, Yeming Wu1, Wenbin Guan2, Wenbo Yan1, Yuhua Li3, Jin Fang3 and Jun Wang1* Abstract Background: Meconium peritonitis is an infrequent congenital disease usually caused by perforation of the fetal digestive tract. Meconium peritonitis resulting from intrauterine appendiceal perforation has been rarely reported and is often overlooked during pregnancy. We herein report two cases of fetal appendiceal perforation. Case presentation: Two neonates were found to have intestinal distension and gradually increasing ascites antenatally. After birth, diagnostic abdominal punctures revealed meconium peritonitis. Urgent surgery showed both neonates had developed gangrenous appendicitis in utero. Pathological examination supported the diagnosis of fetal appendiceal perforation in both neonates, and one also had deformity of cecal duplication. In the present report, we also review the presentation, diagnosis, pathology, management, and recent literature of fetal appendiceal perforation. Conclusion: Meconium peritonitis due to fetal appendiceal perforation is extremely rare, and preoperative diagnosis is almost impossible. However, clinicians should be aware of abnormal gastrointestinal manifestations in the fetus during the antenatal examination. For neonates with severe meconium peritonitis, an early operation with careful intraoperative exploration is necessary. Keywords: Meconium peritonitis, Appendicitis, Intestinal duplication, Fetus, Surgery Background experience with special reference to the clinical presen- Meconium peritonitis (MP) is a sterile chemical periton- tation, evaluation (particularly with respect to the pre- itis that is caused by intrauterine bowel perforation and operative diagnosis and pathological diagnosis), and has low morbidity (1/30,000). -
Endoscopic Treatment of Gastric Volvulus
Case report Endoscopic treatment of gastric volvulus Martín Alonso Gómez, MD,1 Camilo Ortiz, MD.2 1 Assistant Professor of Internal Medicine at the Abstract Universidad Nacional de Colombia. Gastroenterology Unit, Hospital El Tunal. Gastric volvulus is a very rare disease which may be either acute or chronic, and which may be associated 2 General Surgeon. Laparoscopist. Universidad de la with other pathologies. Quick identification of gastric volvulus is very important because the prognosis of the Sabana. Hospital El Tunal. patient depends on opportune treatment. Usually open gastropexy or laparoscopy is performed. Nevertheless, ......................................... endoscopic treatment can be tried since it is faster and simpler and results in less morbidity. Received: 07-04-10 In this article we present two cases of endoscopic devolvulation of gastric volvulus. The technique is descri- Accepted: 01-02-11 bed in detail and we present a review of the literature regarding this strange disease. Keywords Gastric volvulus, endoscopy, hernia. Gastric Volvulus is the abnormal rotation of the stomach CliniCAl CAse 1 on one of its two axes (vertical or horizontal) that leads to the presence of obstructive symptoms such as vomiting The patient was an 81 year old woman with arterial hyper- and abdominal pain. Although this disease is very rare tension, and coronary disease in three arteries. She was it was described in 1866 by Berti, then by Berg in 1895 bedridden due to a stroke which had occurred six months who presented two cases which were successfully treated earlier. The patient was sent to our hospital for treatment through surgery. In 1930 Buchanan described the associa- of an intestinal obstruction. -
Gallbladder Volvulus: a Rare Emergent Cause of Acute Cholecystitis, If Untreated, Progresses to Necrosis and Perforation Justin L
ISSN : 2376-0249 International Journal of Volume 3 • Issue 3• 1000439 Clinical & Medical Imaging March, 2016 http://dx.doi.org/10.4172/2376-0249.1000439 Case Blog Title: Gallbladder Volvulus: A Rare Emergent Cause of Acute Cholecystitis, if Untreated, Progresses to Necrosis and Perforation Justin L. Regner* and Angela Lomas Department of Surgery, Baylor Scott and White Health and Texas A&M Health Science Center College of Medicine, Temple, TX, USA Figure 1: The gallbladder (black in color) volvulized on its pedicle is necrotic in appearance. Figure 2: A different angle of the gallbladder with less manipulation reveals the extent of the torsion and the significant pedunculated origin. Figure 3: Ultrasound imaging revealed gallbladder wall thickening of 5 mm and pericholecystic fluid consistent with acute cholecystitis. Figure 4: Computed tomography axial cross section depicts a dilated gallbladder with wall thickening and pericholecystic fluid present. Figure 5: A coronal cross section CT image reveals the extent of the gallbladder dilation and amount of pericholecystic fluid. Case Presentation An 86 year-old woman with a past medical history significant for abdominal hernia and Alzheimer dementia presented to the Emergency Department with a 24 hour history of acute right upper quadrant pain associated with nausea and non-bilious emesis. Physical exam revealed right sided abdominal tenderness with associated mass. All laboratory values were within normal ranges. Both abdominal ultrasound and computed tomography of the abdomen/pelvis revealed a large distended gallbladder with wall thickening and gallstones. Based on presentation and radiologic findings, the emergency general surgery service was consulted for suspected acute cholecystitis. -
Pulmonary Hypoplasia: Lung Weight and Radial Alveolar Count As Criteria of Diagnosis
Arch Dis Child: first published as 10.1136/adc.54.8.614 on 1 August 1979. Downloaded from Archives of Disease in Childhood, 1979, 54, 614-618 Pulmonary hypoplasia: lung weight and radial alveolar count as criteria of diagnosis S. S. ASKENAZI AND M. PERLMAN Hadassah Hospital, Jerusalem SUmmARY A working definition of pulmonary hypoplasia (PH) was established by retrospective assessment of lung growth both in recognised and hypothetical PH-associated conditions. Lung weight: body weight ratios (LW:BW) were calculated, and morphometry was determined by the radial alveolar count (RAC) (Emery and Mithal, 1960). Both parameters were reduced compared with those of normal controls in diaphragmatic hernia, anencephalus, anuric renal anomalies, chondrodystrophies, and osteogenesis inperfecta. Comparison of LW:BW ratio and RAC indicated that the RAC was the more reliable criterion of PH, LW:BW ratio of .0-012 (67% of mean nor- mal ratio) and/or RAC of < 4.1 (75 % of mean normal count) are suggested as diagnostic criteria of PH. Evidence ofPH was incidentally discovered in a number ofclinically unsuspected cases and retro- spectively clarified the clinical and radiological findings. Routine assessment of lung growth should be an essential part of the neonatal necropsy. Pulmonary hypoplasia (PH) is a poorly defined establish. There has been only one study of both copyright. condition considered to be almost invariably LW:BW ratio and morphometry in a substantial secondary to other anomalies and is usually diag- number of pathological cases (Reale and Esterly, nosed in association with them; primary or isolated 1973). PH has not been reported (Reale and Esterly, 1973).