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[Waldmann disease and pregnancy].

M P Quemere¹, G Descargues, E Verspyck

¹Clinique Gynécologique et Obstétricale, 1, rue de Germont, C.H.U. Charles Nicolle, 76031 Rouen.

Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction

|September 30, 2000

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Waldman disease, or intestinal lymphangiectasis, is a rare genetic disorder affecting nutrient absorption. This case study highlights a successful pregnancy and delivery in a patient with this condition.

Area of Science:

Gastroenterology
Genetics
Obstetrics

Background:

Waldman disease (intestinal lymphangiectasis) is a protein-losing enteropathy stemming from abnormal intestinal lymphatic vessels.
It follows an autosomal dominant inheritance pattern and typically manifests in early childhood.
Management often involves dietary changes, such as medium-chain triglyceride supplementation.

Observation:

This report details a rare case of intestinal lymphangiectasis diagnosed in a pregnant woman.
The patient's pregnancy progressed to a full-term delivery.
No significant complications were noted during the pregnancy or delivery.

Findings:

Intestinal lymphangiectasis can occur during pregnancy without major adverse outcomes for mother or child.

Related Experiment Videos

Successful management and delivery are achievable in pregnant patients with this condition.

Implications:

This case suggests that pregnancy is a viable option for women with Waldman disease.
Further research into managing intestinal lymphangiectasis during pregnancy is warranted.
This finding may offer reassurance to patients with this condition considering pregnancy.