Simple Summary Pancreatic neuroendocrine tumors (pNETs) are rare, indolent cancers
whose causation is only partly understood. An increasing number of studies have uncovered …

Non-coding RNAs (ncRNAs) are known to regulate gene expression at the transcriptional
and post-transcriptional levels, chromatin remodeling, and signal transduction. The …

Objectives: Describe the appearance of a neurofibroma. Explain how to counsel a patient
with multiple cutaneous neurofibromas or a plexiform neurofibroma. Identify management …

Peripheral nerve sheath tumors such as neurofibroma, comprise 5% of all benign soft tissue
tumors and usually occur due to an underlying neurofibromatosis. A plexiform neurofibroma …

Background: type 1 neurofibromatosis (NF1) is the most common neurocutaneous disorder,
and it is an inherited condition that causes a tumour predisposition. Central nervous system …

Plexiform neurofibroma (PNF) is a rare variant of neurofibromatosis type1 (NF-1), which
histopathologically, is a subtype of benign nerve sheath tumors, neurofibromas (NF). It …

Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder.
Clinically, the hallmarks of NF1 include skin pigmentation and cutaneous neurofibroma …

Introduction and importance Neurofibromatosis type 1 is a benign peripheral nerve tumor,
often manifests as plexiform neurofibroma that may cause severe dysfunction, pain, and …

The lacrimal gland is a bilobed serous gland located in the superolateral aspect of the orbit.
Lacrimal system pathologies can be broadly divided into pathologies of the lacrimal gland …

Dr Hamikchandra Patel* Dr Sandeep Rao INTERNATIONAL JOURNAL OF SCIENTIFIC
RESEARCH ABSTRACT KEYWORDS Page 1 ORIGINAL RESEARCH PAPER MODULATION …