Preview

Medical Immunology (Russia)

Advanced search

Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns

https://doi.org/10.15789/1563-0625-SOI-1930

Abstract

Hereditary angioedema (HAE) is a genetically caused orphan disease with a high risk of developing life-threatening attacks, thus requiring availability for up-to-date information on this problem for the doctors of any specialties. A limited number of observations determine the value of the analysis for each clinical case. Many facets of clinical manifestations, a list of predisposing and triggering factors, as well as limitations of some diagnostic and therapeutic algorithms, require the development of individual management schemes under distinct clinical situations. In this paper, we present the unique clinical cases with certain limitations, describing unexpected onset of the disease in the course of pregnancy, management aspects during delivery and post-delivery periods in a women with a previously confirmed HAE diagnosis. Adapted diagnostic algorithms of postnatal diagnostic verification are presented for children with burdened genetic history. We express some assumptions about involvement of a multidisciplinary team of specialists, personalized approach to building a management plan with an “online” correction depending on observation stage of НАЕ patient.

About the Authors

E. N. Bobrikova
Сlinical Hospital No. 52
Russian Federation

Chief District Allergologist, Head, Clinical and Diagnostic Center for Allergology and Immunology

Moscow



A. R. Denisova
First Moscow State I. Sechenov Medical University
Russian Federation

PhD (Medicine), Assistant Professor, Department of Pediatrics, N. Filatov Clinical Institute for Pediatric Health

Moscow



T. S. Kotomina
Сlinical Hospital No. 52
Russian Federation

PhD (Medicine), The Moscow Doctor, Head, Obstetric Department

Moscow



S. A. Serdotetskova
Сlinical Hospital No. 52
Russian Federation

Serdotetskova Sofia A. – Allergist-Immunologist, Center for Allergology and Immunology

123182, Moscow, Pekhotnaya str., 3
Phone: 7 (499) 196-45-65



D. S. Fomina
Сlinical Hospital No. 52; First Moscow State I. Sechenov Medical University
Russian Federation

Phd (Medicine), Chief City AllergologistImmunologist. Associate Professor, Department of Clinical Immunology and Allergology, First Moscow State I. Sechenov Medical University; Head, Allergology and Immunology Center, Сlinical Hospital No. 52

Moscow



References

1. Aabom A., Nguyen D., Fisker N., Bygum A. Health-related quality of life in Danish children with hereditary angioedema. Allergy Asthma Proc., 2017, Vol. 38, no. 6, pp. 440-446.

2. Belbézier A., Hardy G., Marlu R., Defendi F., Dumestre Perard C., Boccon-Gibod I., Launay D., Bouillet L. Plasminogen gene mutation with normal C1 inhibitor hereditary angioedema: Three additional French families. Allergy, 2018, Vol. 73, no. 11, pp. 2237-2239.

3. Bork K., Meng G., Staubach P., Hardt J. Hereditary angioedema: new findings concerning symptoms, affected organs, and course. Am. J. Med., 2006, Vol. 119, no. 3, pp. 267-274.

4. Bork K., Wulff K., Hardt J., Witzke G., Staubach P. Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy. J Allergy Clin. Immunol., 2009, Vol. 124, no. 1, pp. 129-134.

5. Bork K., Wulff K., Steinmüller-Magin L., Braenne I., Staubach-Renz P., Witzke G., Hardt J.Hereditary angioedema with a mutation in the plasminogen gene. Allergy, 2018, Vol. 73, no. 2, pp. 442-450.

6. Bouillet L., Longhurst H., Boccon-Gibod I., Bork K., Bucher C., Bygum A., Caballero T., Drouet C., Farkas H., Massot C., Nielsen E.W., Ponard D., Cicardi M. Disease expression in women with hereditary angioedema. Am. J. Obstet. Gynecol., 2008, Vol. 199, no. 5, pp. 484.e1-484.e4.

7. Bowen T., Cicardi M., Farkas H., Bork K., Longhurst H.J., Zuraw B., Aygoeren-Pürsün E., Craig T., Binkley K., Hebert J., Ritchie B., Bouillet L., Betschel S., Cogar D., Dean J., Devaraj R., Hamed A., Kamra P., Keith P.K., Lacuesta G., Leith E., Lyons H., Mace S., Mako B., Neurath D., Poon M.C., Rivard G.E., Schellenberg R., Rowan D., Rowe A., Stark D., Sur S., Tsai E., Warrington R., Waserman S., Ameratunga R., Bernstein J., Björkander J., Brosz K., Brosz J., Bygum A., Caballero T., Frank M., Fust G., Harmat G., Kanani A., Kreuz W., Levi M., Li H., MartinezSaguer I., Moldovan D., Nagy I., Nielsen E.W., Nordenfelt P., Reshef A., Rusicke E., Smith-Foltz S., Späth P., Varga L., Xiang Z.Y. 2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema. Allergy Asthma Clin Immunol., 2010, Vol. 6, no. 1, 24. doi: 10.1186/1710-1

8. Bygum A. Hereditary angio-oedema in Denmark: a nationwide survey. Br. J. Dermatol., 2009, Vol. 161, pp. 1153-1158.

9. Caballero T., Baeza M.L., Cabañas R., Campos A., Cimbollek S., Gómez-Traseira C., González-Quevedo T., Guilarte M., Jurado-Palomo G.J., Larco J.I., López-Serrano M.C., López-Trascasa M., Marcos C., Muñoz-Caro J.M., Pedrosa M., Prior N., Rubio M., Sala-Cunill A.; Spanish Study Group on Bradykinin-Induced Angioedema; Grupo Español de Estudio del Angioedema mediado por Bradicinina. Consensus statement on the diagnosis, management, and treatment of angioedema mediated by bradykinin. Part I. Classification, epidemiology, pathophysiology, genetics, clinical symptoms, and diagnosis. J. Investig. Allergol. Clin. Immunol., 2011, Vol. 21, no. 5, pp. 333-347.

10. Caballero T., Canabal J., Rivero-Paparoni D., Cabanas R. Management of hereditary angioedema in pregnant women: a review. Int. J. Womens Health, 2014, Vol. 6, pp. 839-848.

11. Caballero T., Farkas H., Bouillet L., Bowen T., Gompel A., Fagerberg C., Bjökander J., Bork K., Bygum A., Cicardi M., de Carolis C., Frank M., Gooi J.H., Longhurst H., Martínez-Saguer I., Nielsen E.W., Obtulowitz K., Perricone R., Prior N; C-1-INH Deficiency Working Group. International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency. J. Allergy Clin. Immunol., 2012, Vol. 129, no. 2, pp. 308-320.

12. Cicardi M., Aberer W., Banerji A., Bas M., Bernstein J.A., Bork K., Caballero T., Farkas H., Grumach A., Kaplan A.P., Riedl M.A., Triggiani M., Zanichelli A., Zuraw B.; HAWK under the patronage of EAACI (European Academy of Allergy and Clinical Immunology).Classification, diagnosis and approach to treatment in angioedema: consensus report from the Hereditary Angioedema International Working Group. Allergy, 2014, Vol. 69, no. 5, pp. 602-616.

13. Colman R.W. Surface-mediated defense reactions. The plasma contact activation system. J. Clin. Invest., 1984, Vol. 73, no. 5, pp. 1249-1253.

14. Czaller I., Visy B., Csuka D., Füst G., Tóth F., Farkas H. The natural history of hereditary angioedema and the impact of treatment with human C1-inhibitor concentrate during pregnancy: a long-term survey. Eur. J. Obstet. Gynecol. Reprod. Biol., 2010, Vol. 152, no. 1, pp. 44-49.

15. Davis C.A., Vallota E.H., Forristal J. Serum complement levels in infancy: age related changes. Pediatr. Res., 1979, Vol. 13. no. 9, pp. 1043-1046.

16. Farkas H., Varga L., Szeplaki G., Visy B., Harmat G., Bowen T. Management of hereditary angioedema in pediatric patients. Pediatrics, 2007, Vol. 120, no. 3, pp. e713-e722.

17. Kaplan A.P., Joseph K. The bradykinin-forming cascade and its role in hereditary angioedema. Ann. Allergy Asthma Immunol., 2010, Vol. 104, no. 3, pp. 193-204.

18. McGlinchey P.G., McCluskey D.R. Hereditary angioedema precipitated by estrogen replacement therapy in a menopausal woman. Am. J. Med. Sci., 2000, Vol. 320, no. 3, pp. 212-213.

19. Nielsen E.W., Johansen H.T., Holt J., Mollnes T.E. C1 inhibitor and diagnosis of hereditary angioedema in newborns. Pediatr. Res., 1994, Vol. 35, no. 2, pp. 184-187.

20. Perricone R., Pasetto N., de Carolis C., Vaquero E., Noccioli G., Panerai A.E., Fontana L. Cystic ovaries in women affected with hereditary angioedema. Clin. Exp. Immunol., 1992, Vol. 90, no. 3, pp. 401-404.

21. Roach B., Kim Y., Jerome E., Michael A.F. Influence of age and sex on serum complement components in children. Am. J. Dis. Child., 1981, Vol. 135, no. 10, pp. 918-920.

22. Sabharwal G., Craig T. Pediatric hereditary angioedema: an update.Version 1. F1000Res., 2017, Vol. 6, pii: F1000 Faculty Rev-1205. doi: 10.12688/f1000research.11320.1.

23. Zuraw B.L., Bork K., Binkley K.E., Banerji A., Christiansen S.C., Castaldo A., Kaplan A., Riedl M., Kirkpatrick C., Magerl M., Drouet C., Cicardi M. Hereditary angioedema with normal C1 inhibitor function: consensus of an international expert panel. Allergy Asthma Proc., 2012, Vol. 33, Suppl. 1, pp. S145-S156.

24. Zuraw B.L. Clinical practice. Hereditary angioedema. N. Engl. J. Med., 2008, Vol. 359, no. 10, pp. 1027-1036.


Supplementary files

1. Литература
Subject
Type Исследовательские инструменты
Download (18KB)    
Indexing metadata ▾
2. Метаданные
Subject
Type Исследовательские инструменты
Download (14KB)    
Indexing metadata ▾
3. Подписи авторов
Subject
Type Исследовательские инструменты
View (842KB)    
Indexing metadata ▾
4. Резюме
Subject
Type Исследовательские инструменты
Download (13KB)    
Indexing metadata ▾
5. Титульный лист
Subject
Type Исследовательские инструменты
Download (17KB)    
Indexing metadata ▾
6. Текст статьи (дубликат)
Subject
Type Исследовательские инструменты
Download (40KB)    
Indexing metadata ▾

Review

For citations:


Bobrikova E.N., Denisova A.R., Kotomina T.S., Serdotetskova S.A., Fomina D.S. Significance of individual management plan for the patients with hereditary lymphangioedema during pregnancy and lactation, and in newborns. Medical Immunology (Russia). 2020;22(3):577-584. (In Russ.) https://doi.org/10.15789/1563-0625-SOI-1930

Views: 759


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1563-0625 (Print)
ISSN 2313-741X (Online)