Case Report: Stüve-Wiedemann syndrome-a rare cause of persistent pulmonary hypertension of the newborn

被引:1
作者
Jin, Jessica [1 ]
Rothaemel, Paula [1 ]
Buechel, Johanna [2 ]
Kammer, Birgit [3 ]
Brunet, Theresa [4 ]
Pattathu, Joseph [5 ]
Flemmer, Andreas W. [1 ]
Nussbaum, Claudia [1 ]
Schroepf, Sebastian [1 ]
机构
[1] Ludwig Maximilians Univ Munchen, Univ Hosp, Dr Von Hauner Childrens Hosp, Div Neonatol,Dept Pediat, Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Univ Hosp, Clin & Outpatient Clin Obstet & Gynecol, Munich, Germany
[3] Ludwig Maximilians Univ Munchen, Univ Hosp, Dr Von Hauner Childrens Hosp, Dept Pediat Radiol, Munich, Germany
[4] Tech Univ Munich, Univ Hosp, Inst Human Genet, Klinikum Rechts Isar, Munich, Germany
[5] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Pediat Cardiol & Pediat Intens Care, Munich, Germany
来源
FRONTIERS IN PEDIATRICS | 2024年 / 11卷
关键词
case report; Stuve-Wiedemann syndrome; PPHN; limb abnormalities; whole exome sequencing; STUVE-WIEDEMANN-SYNDROME; TYPE-2;
D O I
10.3389/fped.2023.1329404
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
IntroductionPersistent pulmonary hypertension of the newborn (PPHN) is a life-threatening condition characterized by hypoxemia due to elevated pulmonary vascular resistance. PPHN commonly arises secondary to various underlying conditions, including infection, meconium aspiration, and respiratory distress syndrome. Management includes pulmonary vasodilators, mechanical ventilation, oxygen supplementation, vasopressors, and volume replacement. Stuve-Wiedemann syndrome (SWS), a rare genetic disorder characterized by bone dysplasia, respiratory distress, hyperthermia, and swallowing difficulties, may present with pulmonary hypertension, indicating a poor prognosis.Case descriptionA term female neonate presented with secondary respiratory failure and severe PPHN of unknown etiology on the second day of life, necessitating intubation. Clinical findings included facial dysmorphia, camptodactyly, skeletal anomalies, and generalized muscular hypotonia. High-frequency oscillation ventilation and surfactant administration yielded marginal improvement. On the third day of life, a severe pulmonary hypertensive crisis necessitated inhaled and systemic pulmonary vasodilators along with volume and catecholamine therapy. Whole exome sequencing revealed a homozygous mutation in the leukemia inhibitory factor receptor (LIFR) gene, consistent with Stuve-Wiedemann syndrome.Discussion/conclusionThe case underscores the importance of considering and prompting evaluation of rare genetic causes in the differential diagnosis of PPHN, especially when other abnormalities are present and conventional therapies prove inadequate. Therapeutic strategies must account for the different pathophysiology of primary PPHN including vascular remodeling, as seen in SWS, which may not respond to pulmonary vasodilators typically employed in secondary PPHN due to vasoconstriction. In this case, the patient responded well to treatment for primary PPHN, but the use of high-frequency oscillation ventilation and surfactant was not helpful.
引用
收藏
页数:6
相关论文
共 50 条
  • [11] An uncommon cause of a common disease: a case report of a rare cause of hypertension
    Rao, Sarita
    Rao, Roshan
    Kumar, Achukatla
    Benjamin, Nitika
    Pandey, Akshat
    [J]. EUROPEAN HEART JOURNAL-CASE REPORTS, 2024, 8 (10)
  • [12] Hydralazine induced vasculitis with pulmonary-renal syndrome-A case report
    Andrew Jeyaruban
    Elizabeth Downie
    Kasim A. Ismail
    Hari Nandakoban
    [J]. SN Comprehensive Clinical Medicine, 5 (1)
  • [13] Intravascular B-cell lymphoma: case report of a rare cause of pulmonary arterial hypertension
    Share, Michael
    Giannini, Gabriel
    Kim, Stacey
    Singh, Siddharth
    [J]. EUROPEAN HEART JOURNAL-CASE REPORTS, 2019, 3 (01)
  • [14] An unexpected cause of pulmonary hypertension in a young woman: a case report
    Aeberhard, Judith
    Lichtblau, Mona
    Arenja, Nisha
    [J]. EUROPEAN HEART JOURNAL-CASE REPORTS, 2023, 7 (10)
  • [15] Persistent Pulmonary Hypertension of the Newborn Secondary to Labile Hypoxemia Associated With Cyanosis: A Case Series
    Bhagwat, Anushka P.
    Sharath, H., V
    Seth, Nikita H.
    Puri, Saurabh N.
    [J]. CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (02)
  • [16] Transient Myeloproliferative Disorder in a Neonate without Down Syndrome-A Rare Case Report and Review of the Literature
    Vellatt, Devaki Menon Kizhakke
    Jayaraman, Dhaarani
    Amuthan, Shwetha
    Balakrishnan, Umamaheswari
    Koshy, Teena
    Subramanian, Arun Kumar
    Scott, Julius Xavier
    [J]. INDIAN JOURNAL OF MEDICAL AND PAEDIATRIC ONCOLOGY, 2024,
  • [17] Abdominal cocoon syndrome as rare cause of intestinal obstruction: A case report
    Mousavi, Mir Ali
    Shaghaghi, Ali
    Sabouri, Mohammad
    Yousefian, Roya
    [J]. INTERNATIONAL JOURNAL OF SURGERY CASE REPORTS, 2022, 98
  • [18] Rare urogenital malformation with prune belly syndrome in a newborn female: A case report
    Elhafid, Melanie
    Milbrandt, Kristopher
    [J]. JOURNAL OF PEDIATRIC SURGERY CASE REPORTS, 2025, 115
  • [19] Type II Abernethy malformation in an adult male patient—a rare and reversible cause of pulmonary hypertension: a case report with review of literature
    Arjun Agarwal
    Durvesh Bhangale
    Vinayak M. Sawardekar
    Srikar Puvvada
    [J]. The Egyptian Journal of Internal Medicine, 2021, 33
  • [20] Reversal of pulmonary arterial hypertension in POEMS syndrome with thalidomide: a case report
    Tanaka, Toshikazu D.
    Misawa, Sonoko
    Yoshimura, Michihiro
    Kuwabara, Satoshi
    [J]. EUROPEAN HEART JOURNAL-CASE REPORTS, 2018, 2 (02)