Comorbidity: alobar holoprosencephaly and pulmonary tuberculosis in a child (a case report)

Authors

DOI:

https://doi.org/10.14739/2310-1210.2023.6.288828

Keywords:

alobar holoprosencephaly, pulmonary tuberculosis, child, household, clinical case

Abstract

Aim: to demonstrate the features of detection and management of a child with simultaneous alobar holoprosencephaly and pulmonary tuberculosis (TB) by the example from our own clinical observation.

Materials and methods. A clinical case of our own observation of the simultaneous course of pulmonary TB and alobar holoprosencephaly in the child who was treated in the pediatric department of the clinical base of the Department of Phthysiatry and Pulmonology of Zaporizhzhia State Medical and Pharmaceutical University on Public Non-Profit Enterprise “Zaporizhzhia Regional Clinical and Diagnostic Center of Phthysiatry and Pulmonology” of Zaporizhzhia Regional Council.

Results. The 4-year-old child diagnosed with pulmonary TB was admitted to the Pediatric Department. Previously, the child was diagnosed with alobar holoprosencephaly in a children’s hospital. His condition was severe due to the main disease. Family members, who had contact with the child, were examined to rule out TB. The index patient was a grandmother, who had recurrent drug-sensitive TB and was looking after the child living apart from the family. The treatment for TB was successful, but the child developed drug-induced hepatotoxicity. Also, the child had episodic convulsions when admitted to the department, which did not repeat after the prescribed treatment by a neurologist.

Conclusions. Alobar holoprosencephaly is a severe and rare structural brain abnormality with complex and multifactorial causes. This condition can be identified at the first screening examination of a pregnant woman, so prenatal diagnosis is quite important. The disease leads to severe disability and requires assistance of physicians in different specialties. Treatment for tuberculosis is successful but demands more monitoring of side effects during antimycobacterial therapy.

Author Biographies

Yu. V. Myronchuk, Zaporizhzhia State Medical and Pharmaceutical University, Ukraine

MD, PhD, Assistant of the Department of Phthisiology and Pulmonology

O. O. Pushnova, PNE “Zaporizhzhia Regional Clinical and Diagnostic Center of Phthysiatry and Pulmonology” ZRC, Ukraine

MD, Pediatric Phthisiatrician

L. V. Taran, PNE “Zaporizhzhia Regional Clinical and Diagnostic Center of Phthysiatry and Pulmonology” ZRC, Ukraine

Pediatric Phthisiatrician

O. V. Dvizov, PNE “Zaporizhzhia Regional Clinical and Diagnostic Center of Phthysiatry and Pulmonology” ZRC, Ukraine

MD, Radiologist

References

Society for Maternal-Fetal Medicine (SMFM), & Monteagudo, A. (2020). Holoprosencephaly. American journal of obstetrics and gynecology, 223(6), B13-B16. https://doi.org/10.1016/j.ajog.2020.08.178

Nakawa, W., Alkhalil, S., Martini, N., & Alawad, I. (2023). Rare manifestations of alobar holoprosencephaly and the potential causes: a report of two cases. Annals of medicine and surgery (2012), 85(2), 252-256. https://doi.org/10.1097/MS9.0000000000000176

Ionescu, C. A., Vladareanu, S., Tudorache, S., Ples, L., Herghelegiu, C., Neacsu, A., Navolan, D., Dragan, I., & Oprescu, D. N. (2019). The wide spectrum of ultrasound diagnosis of holoprosencephaly. Medical ultrasonography, 21(2), 163-169. https://doi.org/10.11152/mu-1614

Honey, E. M., Bütow, K. W., & Zwahlen, R. A. (2019). Holoprosencephaly with Clefts: Data of 85 Patients, Treatment and Outcome: Part 1: History, Subdivisions, and Data on 85 Holoprosencephalic Cleft Patients. Annals of maxillofacial surgery, 9(1), 140-145. https://doi.org/10.4103/ams.ams_50_19

Meryem, B., Amine, N., Houssein, O., Siham, E. H., Nazik, A., & Latifa, C. (2023). Antenatal and Postnatal Diagnosis of Semilobar Holoprosencephaly: Two Case Reports. Global pediatric health, 10, 2333794X231156037. https://doi.org/10.1177/2333794X231156037

El-Dessouky, S. H., Aboulghar, M. M., Gaafar, H. M., Abdella, R. M., Sharaf, M. F., Ateya, M. I., Elarab, A. E., Zidan, W. H., Helal, R. M., Aboelsaud, S. M., Eid, M. M., & Abdel-Salam, G. M. H. (2020). Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations. Prenatal diagnosis, 40(5), 565-576. https://doi.org/10.1002/pd.5649

Volpe, N., Dall'Asta, A., Di Pasquo, E., Frusca, T., & Ghi, T. (2021). First-trimester fetal neurosonography: technique and diagnostic potential. Ultrasound in obstetrics & gynecology, 57(2), 204-214. https://doi.org/10.1002/uog.23149

Ariyo, I. J., Mchaile, D. N., Magwizi, M., Kayuza, M., Mrindoko, P., & Chussi, D. C. (2022). Alobar holoprosencephaly with cebocephaly in a neonate: A rare case report from Northern Tanzania. International journal of surgery case reports, 93, 106960. https://doi.org/10.1016/j.ijscr.2022.106960

Montaguti, E., Cariello, L., Brunelli, E., Youssef, A., Livi, A., Salsi, G., & Pilu, G. (2022). Sonography of fetal holopr osencephaly: a guide to recognize the lesser varieties. The journal of maternal-fetal & neonatal medicine, 35(25), 9717-9723. https://doi.org/10.1080/14767058.2022.2050900

Hu, Y., Sun, L., Feng, L., Wang, J., Zhu, Y., & Wu, Q. (2023). The role of routine first-trimester ultrasound screening for central nervous system abnormalities: a longitudinal single-center study using an unselected cohort with 3-year experience. BMC pregnancy and childbirth, 23(1), 312. https://doi.org/10.1186/s12884-023-05644-z

Malta, M., AlMutiri, R., Martin, C. S., & Srour, M. (2023). Holoprosencephaly: Review of Embryology, Clinical Phenotypes, Etiology and Management. Children, 10(4), 647. https://doi.org/10.3390/children10040647

Elfarawi, H., Tolusso, L., McGowan, M. L., Cortezzo, D., & Vawter-Lee, M. (2022). Alobar holoprosencephaly: Exploring mothers' perspectives on prenatal decision-making and prognostication. Prenatal diagnosis, 42(5), 617-627. https://doi.org/10.1002/pd.6130

World Health Organization. (2018). Latent tuberculosis infection: updated and consolidated guidelines for programmatic management. Retrieved from https://apps.who.int/iris/handle/10665/260233

Weiss, K., Kruszka, P., Guillen Sacoto, M. J., Addissie, Y. A., Hadley, D. W., Hadsall, C. K., Stokes, B., Hu, P., Roessler, E., Solomon, B., Wiggs, E., Thurm, A., Hufnagel, R. B., Zein, W. M., Hahn, J. S., Stashinko, E., Levey, E., Baldwin, D., Clegg, N. J., Delgado, M. R., … Muenke, M. (2018). In-depth investigations of adolescents and adults with holoprosencephaly identify unique characteristics. Genetics in medicine, 20(1), 14-23. https://doi.org/10.1038/gim.2017.68

Weiss, K., Kruszka, P. S., Levey, E., & Muenke, M. (2018). Holoprosencephaly from conception to adulthood. American journal of medical genetics. Part C, Seminars in medical genetics, 178(2), 122-127. https://doi.org/10.1002/ajmg.c.31624

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Published

2023-12-05

How to Cite

1.
Myronchuk YV, Pushnova OO, Taran LV, Dvizov OV. Comorbidity: alobar holoprosencephaly and pulmonary tuberculosis in a child (a case report). Zaporozhye Medical Journal [Internet]. 2023Dec.5 [cited 2024Nov.26];25(6):563-70. Available from: http://zmj.zsmu.edu.ua/article/view/288828