Gaucher’s Disease


A 73-year-old man presented to the emergency department with a 1-month history of fatigue and diffuse bone pain. He reported no abdominal pain or neurologic symptoms. On physical examination, there was no hepatosplenomegaly. Laboratory studies showed a white-cell count of 1700 per cubic millimeter (reference range, 4000 to 10,000), a hemoglobin level of 5.9 g per deciliter (reference range, 12 to 18), and a platelet count of 111,000 per cubic millimeter (reference range, 120,000 to 180,000). Whole-body magnetic resonance imaging revealed osteonecrosis of the right humerus and right femur. Bone marrow biopsy revealed macrophages with a “wrinkled tissue paper” appearance in the cytoplasm (arrow, May–Grünwald Giemsa staining), a finding consistent with Gaucher’s cells. Further testing identified reduced β-glucocerebrosidase activity and homozygosity with the N370S variant of the GBA gene. Workup for hematologic cancers was negative. A diagnosis of type 1 Gaucher’s disease was made. Gaucher’s disease is an autosomal recessive disease that results in a deficiency of the lysosomal enzyme β-glucocerebrosidase. In type 1 Gaucher’s disease, some patients do not present with symptoms until late adulthood. Clinical features include fatigue, hepatosplenomegaly, pancytopenia, bone pain, osteonecrosis, and — in children — growth retardation. The patient began receiving enzyme-replacement therapy. At 6 months of follow-up, his symptoms had abated and cell counts had improved.

A Newborn with Thrombocytopenia, Cataracts, and Hepatosplenomegaly


http://www.nejm.org/doi/full/10.1056/NEJMcpc1706110?utm_medium=referral&utm_source=r360

A Newborn with Thrombocytopenia, Cataracts, and Hepatosplenomegaly


How common is the use of the rubella vaccine worldwide?

The acronym TORCH (toxoplasmosis, other [syphilis, varicella, parvovirus B19 infection, HIV infection], rubella, cytomegalovirus infection, and herpes simplex virus infection) is often used to identify possible congenital infections.

Clinical Pearls

Q: What are some of the clinical manifestations of the congenital rubella syndrome?

A: Cataracts, thrombocytopenia, bony abnormalities, and deafness are consistent with the congenital rubella syndrome.

Table 2. (10.1056/NEJMcpc1706110/T2) Manifestations of the Congenital Rubella Syndrome.

Q: How is the congenital rubella syndrome diagnosed?

A: Newborns with the congenital rubella syndrome shed rubella virus in the throat, nasopharynx, and urine. Because growth of the virus in cultured mammalian cell lines is relatively slow and cultivation and identification of the virus are labor-intensive, nucleic acid amplification tests have been developed to directly detect rubella virus RNA in clinical samples.

Morning Report Questions

Q: Can serologic testing also establish the diagnosis of the congenital rubella syndrome?

A: In addition to direct viral detection, evidence of the production of antibodies to rubella virus in an infant can be used to establish a diagnosis of the congenital rubella syndrome. Affected newborns produce IgM antibodies to rubella virus. These antibodies can usually be detected at birth with the use of a capture enzyme-linked immunosorbent assay; the level increases during the first 3 months of life and then declines over time. At birth, tests for IgG antibodies to rubella virus cannot be used to distinguish between transplacentally acquired maternal antibodies and antibodies produced by the neonate. However, another means of establishing a diagnosis of the congenital rubella syndrome is showing that the level of IgG antibodies to rubella virus does not substantially decrease during the first few months of life, as the maternal antibodies decay. Finally, IgG antibodies to rubella virus that are produced by infants with congenital infection are typically of low avidity; therefore, a diagnosis of the congenital rubella syndrome can be established by detecting low-avidity antibodies in the blood after the maternal antibodies have waned.

Q: How common is use of the rubella vaccine worldwide?

A: The estimated number of cases of the congenital rubella syndrome worldwide is still approximately 100,000 per year. Rubella and the congenital rubella syndrome have been eradicated from the Western hemisphere because of good vaccine coverage. Unfortunately, although rubella has been controlled in many countries in Europe, opposition to vaccination in some countries has prevented the elimination of rubella, and there is much work to be done. In contrast, routine vaccination against rubella has just begun in some Asian countries, including India, Thailand, China, Japan, and Indonesia. Coverage in Africa is spotty, but a few countries have introduced the vaccine. In Nigeria, vaccination is limited to private providers, and coverage is less than 10%. There is a campaign to introduce the combined measles–rubella vaccine throughout the world, and all regions have goals to eradicate both diseases.