Bilateral proptosis and bitemporal swelling: A rare manifestation of acute myeloid leukemia [0.03%]
双侧突眼及双侧颞部肿胀：急性髓系白血病的罕见表现
Dinesh Rajput,Ram Naval,Kamlesh Yadav et al.
Dinesh Rajput et al.
Background: In Acute Myeloid Leukemia (AML), malignant clones of immature myeloid cells (primarily blasts) proliferate, replace bone marrow, circulate in blood and invade other tissues. The unique presentation of bilatera...
Paternally derived translocation t(8;18)(q22.1;q22)pat associated in a patient with developmental delay: Case report and review [0.03%]
父系衍生易位t（8;18）（q22.1;q22）.pat与发育迟缓相关：病例报告和综述
Lakshmi Rao,Murthy Kanakavalli,Venkata Padmalatha et al.
Lakshmi Rao et al.
The common cause of mental impairment and the wide range of physical abnormalities is balanced chromosome rearrangement. As such, it is difficult to interpret, posing as a diagnostic challenge in human development. We present a unique famil...
Elephantiasis neuromatosa of the lower limb in a patient with neurofibromatosis type-1: A case report with imaging findings [0.03%]
神经纤维瘤病Ⅰ型伴象皮 Neuromatous 神经纤维瘤病的临床及影像学表现：1 例报告
Shahina Bano,Akhila Prasad,Sachchida Nand Yadav et al.
Shahina Bano et al.
Elephantiasis neuromatosa is the most impressive manifestation of neurofibromatosis type-1 (NF-1). We report a case of NF-1 who presented with elephantiasis neuromatosa of his right leg. Cross-sectional imaging not only assists in the corre...
H Gopakumar,R Sivji,P K Rajiv
H Gopakumar
It is presently a universal practice to administer vitamin K at birth. Hence, the serious bleeding manifestations from vitamin K deficiency are nowadays very rare. We describe a case of late vitamin K deficiency bleeding presenting as intra...
Multiple neural tube defects in the same patient with no neurological deficit [0.03%]
同一患者伴有多种神经管畸形但无神经功能缺损
Arun Tungaria,Arun Kumar Srivastav,Ashok K Mahapatra et al.
Arun Tungaria et al.
Congenital deformities involving the coverings of the nervous system are called neural tube defects (NTDs). NTD can be classified as neurulation defects, which occur by stage 12, and postneurulation defects. Cervical meningocele and myelome...
Intramedullary spinal epidermoid cyst of the cervicodorsal region: A rare entity [0.03%]
颈椎和胸椎区域脊髓内表皮样囊肿：一种罕见病症
Ashok Kumar,Pritish Singh,Pramod Jain et al.
Ashok Kumar et al.
Intramedullary spinal epidermoid cysts are rare, with only few cases having been reported in the literature. We are reporting a case of a 10-year-old female child who presented with symptoms of meningitis with progressive paraparesis. Magne...
Dinesh K Rajput,Anant Mehrotra,Arun K Srivastav et al.
Dinesh K Rajput et al.
Bithalamic gliomas are extremely rare tumors of central nervous system. Although they are usually benign in nature, their outcome is poor because of the involvement of thalamic nuclei and inadequate surgical excision. Surgery is usually don...
Desmoplastic infantile ganglioglioma: Report of a case and review of the literature [0.03%]
婴儿期丛状婴幼儿型神经节胶质瘤的病例报告及文献复习
Bita Geramizadeh,Ahmad Kamgarpour,Ali Moradi
Bita Geramizadeh
Desmoplastic infantile ganglioglioma (DIG) is a rare supratentorial brain tumor occurring mostly before the age of 2 years. It has a good prognosis and total excision of the tumor is curative, necessitating no further treatment. An accurate...
R B Kamble,N K Venkataramana,L Naik et al.
R B Kamble et al.
We present a rare case of right parietal sinus pericranii in a 2-year-old female child who presented with a compressible swelling on the right side of the scalp since 3 months of age, with a large head. Magnetic resonance imaging along with...
Zohreh Habibi,Farideh Nejat,Mostafa El Khashab
Zohreh Habibi
Seizure after laminectomy for spinal procedure is very rare and has not been reported after lipomyelomeningocele surgery beforehand. Here, two cases of seizure following laminectomy for lipomyelomeningocele are reported. The exact etiology ...