ABSTRACT
Morgagni’s hernia is rare in pediatrics, representing 1%-6% of all congenital diaphragmatic hernias (CDH). We report a young boy presented with obstructive jaundice caused by compression of common bile duct (CBD) due to stretching and rotation of second part of duodenum in right-sided Morgagni hernia. Such presentation is rarely reported in literature.
ABSTRACT
Introduction Incidence of community acquired methicillin resistant staphylococcus aureus (CA-MRSA) is increasing. Toxic shock syndrome (TSS), Necrotizing fasciitis (NF), Symmetrical peripheral gangrene (SPG) as a manifestation of CA-MRSA are rare in pediatrics. Case Presentation We report a young boy who presented with TSS, NF and SPG by CA-MRSA following trauma. Conclusion CA-MRSA should be taken into consideration as an etiology for these type of clinical presentations. Early and aggressive surgical and medical intervention are the cornerstone for successful management.
ABSTRACT
A 7 year girl presented with history of recurrent vomiting and altered sensonium. Laboratory investigators were within normal limits. A diagnosis of cyclic vomiting syndrome was made and treated with amitryptiline with good results.
Subject(s)
Adrenergic Uptake Inhibitors/therapeutic use , Amitriptyline/therapeutic use , Child , Female , Humans , Periodicity , Syndrome , Vomiting/diagnosis , Vomiting/drug therapy , Vomiting/prevention & controlABSTRACT
Thymomas are associated with various autoimmune disorders in adults, most commonly with myasthenia gravis (MG). In MG antibodies developed against acetylcholine (ACh) receptors, resulting weakness of muscle after repeated use and recovery following a period of rest. However, MG due to thymoma is extremely rare in pediatric age group.1We report an infant with MG due to invasive thymoma.
Subject(s)
Biopsy, Needle , Follow-Up Studies , Humans , Immunohistochemistry , Infant , Male , Myasthenia Gravis/complications , Myasthenia Gravis/diagnostic imaging , Myasthenia Gravis/therapy , Risk Assessment , Severity of Illness Index , Thymectomy/methods , Thymoma/complications , Thymoma/diagnostic imaging , Thymoma/surgery , Thymus Neoplasms/complications , Thymus Neoplasms/diagnosis , Thymus Neoplasms/surgery , Tomography, X-Ray Computed , Treatment OutcomeABSTRACT
We present two cases where GS was sole presentations, months before the diagnosis of AML.