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(C) Cropped orthopantomogram of right ... Intraoral examination was not remarkable. Orthopantomogram demonstrated bilateral multiple cyst like radiolucencies in the region of angle of mandible (figure 1B�CD). Anterioinferior displacement of mandibular second molars was also seen (figure 1B�CD). On the basis of clinical and radiographic features, diagnosis of cherubism was made. Cherubism is a non-neoplastic hereditary bone lesion characterised by a bilateral, painless swelling of the  maxilla and mandible resulting in a fullness of the cheeks and [https://en.wikipedia.org/wiki/Meprobamate meprobamate] retraction of the lower eyelids giving an upward turned appearance of the eyes comparable with a cherub angel.1 2 A molecular pathogenesis of cherubism has been proposed, with the detection of a mutation in the gene encoding SH3-binding protein 2 (SH3BP2) and possible degradation of the Msx-1 gene which is involved in the regulation of mesenchymal interaction during craniofacial morphogenesis.1 It is believed that the different clinical manifestations of cherubism are due to the changes secondary to mutations or incomplete penetrance. Ramon and Engelberg3 proposed a grading system for cherubism Grade 1��involvement of both mandibular ascending rami (as seen in our  patient); Grade 2��grade 1 plus involvement of both maxillary tuberosities; Grade 3��massive involvement of whole maxilla and mandible, except the condylar processes; Grade 4��grade 3 with involvement of the floor of the orbits causing orbital compression. The initial clinical signs of this disease usually begin at about 2?years of age, followed by accelerated growth from 8 to 9?years  and spontaneous interruption after puberty. Being a self-limiting condition, treatment (liposuction and curettage) is mainly for the aesthetics.1 4 Learning points Cherubism classically presents as bilateral, multiple, multilocular, multicystic appearing expansile lesion affecting the jaw bones. Other features are expansion, thinning of cortices and displacement of teeth. The locules are almost always multiple with well-defined septa in between. The disappearance of internal loculation is a sign of resolution.1 Mutation in SH3BP2 and Msx-1 gene are likely to be responsible for cherubism. It may be associated with syndromes like neurofibromatosis type 1, Noonan-like/multiple giant cell lesion syndrome, Ramon syndrome and Jaffe-Campanacci syndrome. Footnotes Competing interests: None. Patient consent: Obtained. Provenance and peer review: Not commissioned; externally peer reviewed.""A 33-year-old woman with a history of an atrioseptal defect (ASD) repaired at age 26, systemic lupus erythematosus on chronic steroids, presented with renal insufficiency and respiratory distress. The patient required intubation, mechanical ventilatory support and haemodynamic support with vasopressors. Fluid therapy was limited because of the presence of pulmonary oedema.