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Damage to the esophagus in combination with hereditary motor and sensory neuropathy: description of a clinical case in a 12-year-old child

https://doi.org/10.31146/1682-8658-ecg-215-7-170-176

Abstract

The article discusses a clinical case of a combination of achalasia of the cardia complicated by candidal esophagitis, which led to severe dysphagia and a significant decrease in body weight of a patient suffering from hereditary motor and sensory neuropathy - Charcot-Marie-Tooth disease (CMT) type 4 E. The authors highlight the pathogenesis and clinical picture diseases, features of the course of achalasia in a patient with a hereditary neurological disease. In this clinical case, an example of a disease in a 12-year-old girl is considered. A feature of this patient was progressive dysphagia, which ultimately led to the almost complete impossibility of normal food intake and the development of nutritional insufficiency. CMT disease is a heterogeneous group of hereditary disorders affecting the peripheral nervous system, as a result of the progression of the disease, motor and sensory dysfunction develops, such patients are under the supervision of neurologists. The presence of atypical symptoms, including not only progressive muscle weakness and exhaustion, with sensory deficits in the distal parts of the limbs, but also the severity of dysphagia, which from episodic becomes permanent, prevents the passage of not only solid food, but also liquid through the esophagus, the occurrence of esophageal vomiting - should serve as the basis for a complete examination of the patient using methods that allow visualization of the esophagus. In the available domestic literature, no description of the combined course of the pathological conditions indicated in the observation was found; isolated cases are given in the foreign literature, so the description of this clinical observation is relevant for raising awareness and early diagnosis of gastrointestinal smooth muscle dysfunction against the background of polyneuropathy.

About the Authors

G. N. Yankina
Siberian state medical University
Russian Federation


E. V. Loshkova
Siberian state medical University; Reasearch Clinical Institute of Childhood of the Ministry of Health of the Moscow Region
Russian Federation


A. I. Khavkin
Reasearch Clinical Institute of Childhood of the Ministry of Health of the Moscow Region; Russian National Research Medical University named after N. I. Pirogov
Russian Federation


I. V. Doroshenko
Siberian state medical University
Russian Federation


M. V. Rebrienko
Siberian state medical University
Russian Federation


Yu. S. Rafikova
Siberian state medical University
Russian Federation


E. I. Kondratieva
Reasearch Clinical Institute of Childhood of the Ministry of Health of the Moscow Region; Federal state budgetary Scientific institution Medical Genetic Research Center named after Academican N. P. Bochkov
Russian Federation


N. D. Odinaeva
Reasearch Clinical Institute of Childhood of the Ministry of Health of the Moscow Region
Russian Federation


V. A. Zhelev
Siberian state medical University
Russian Federation


E. V. Golikova
Siberian state medical University
Russian Federation


A. L. Solnyshko
Siberian state medical University
Russian Federation


T. S. Liulka
Siberian state medical University
Russian Federation


E. A. Bozhenko
Siberian state medical University
Russian Federation


V. K. Prudnikova
Siberian state medical University
Russian Federation


L. V. Kim
Siberian state medical University
Russian Federation


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Review

For citations:


Yankina G.N., Loshkova E.V., Khavkin A.I., Doroshenko I.V., Rebrienko M.V., Rafikova Yu.S., Kondratieva E.I., Odinaeva N.D., Zhelev V.A., Golikova E.V., Solnyshko A.L., Liulka T.S., Bozhenko E.A., Prudnikova V.K., Kim L.V. Damage to the esophagus in combination with hereditary motor and sensory neuropathy: description of a clinical case in a 12-year-old child. Experimental and Clinical Gastroenterology. 2023;(7):170-176. (In Russ.) https://doi.org/10.31146/1682-8658-ecg-215-7-170-176

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