1. The curious incident of a cavum velum interpositum cyst in twins of a mother carrying May-Hegglin anomaly: a case report and short literature review
- Author
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Letizia Di Meglio, Giulio Giordano, Mariano Intrieri, Mario Mastroianno, Giovanni Luca Tiscia, Maurizio Margaglione, Giovanni Favuzzi, Elena Chinni, and Elvira Grandone
- Subjects
Adult ,Pediatrics ,medicine.medical_specialty ,Cavum veli interpositi ,Hearing Loss, Sensorineural ,lcsh:Gynecology and obstetrics ,Ultrasonography, Prenatal ,03 medical and health sciences ,0302 clinical medicine ,Pregnancy ,Case report ,medicine ,Humans ,Cyst ,Peripartum Period ,Twin Pregnancy ,lcsh:RG1-991 ,030304 developmental biology ,Third Ventricle ,Outcome ,0303 health sciences ,030219 obstetrics & reproductive medicine ,Third ventricle ,business.industry ,Cysts ,Infant, Newborn ,Pregnancy Outcome ,Obstetrics and Gynecology ,May-Hegglin ,medicine.disease ,Thrombocytopenia ,Pregnancy Complications ,medicine.anatomical_structure ,May–Hegglin anomaly ,Pregnancy, Twin ,Female ,Psychomotor disorder ,business - Abstract
Background May-Hegglin anomaly is an autosomal dominant inherited condition, characterized by thrombocytopenia, giant platelets and Dohle-like bodies. Incidence is unknown and affected individuals can show from mild to moderate-severe haemorrhagic symptoms. The cyst of cavum veli interpositi (a virtual space filled with fluid within the third ventricle) is rarely reported in the foetal period. Furthermore, it is unclear whether isolated cavum veli interpositi cysts are a normal variant or developmental malformations. The simultaneous presence of these two anomalies was never described. Case presentation We describe a very rare case of a twin monochorionic pregnancy in a woman with the May-Hegglin anomaly, whose foetuses carried cavum veli interpositi cysts. Since childhood, our patient had shown macro-thrombocytopenia, deafness and bleeding (epistaxis and menorrhagia), but she was misdiagnosed until the age of 30 years when our Centre identified a de novo allelic variant in the gene MYH9 coding for the non-muscle myosin heavy chain IIa. Our patient bled neither during the pregnancy, nor in the peripartum period. Children are now eight-months-old and have never bled, although both inherited the MYH9 variant and have thrombocytopenia with giant platelets. Furthermore, none of them developed psychomotor disorders. Conclusions To the best of our knowledge, this is the sixth case of twin pregnancy in a woman carrying May-Hegglin anomaly and the first one with cavum veli interpositi cysts in the neonates. We speculate that MYH9 could have, at least in part, played a role in the development of both conditions, as this gene has a pleiotropic effect.
- Published
- 2020