Paraganglioma of the larynx is a rare neoplasm which mostly arises from supraglottic area.  Herein, we report on a 45-year-old woman presented with supraglottic laryngeal paraganglioma.

Sweet’s syndrome and erythema nodosum are rarely seen together. Herein, we report a case of concurrent Sweet’s syndrome and erythema nodosum and review previous cases.

paraganglioma of the larynx is a rare neoplasm which mostly arises from supraglottic area.  herein, we report on a 45-year-old woman presented with supraglottic laryngeal paraganglioma.

Focal dermal hypoplasia or Goltz syndrome is a rare genodermatosis involving all three embryonic layers. Herein, the first case of this syndrome from Iran will be reported. The main clinical features were fat herniation, reticulate pigmentations, telangiectasia, and skeletal defects.

Human parvovirus (HPV) B19 induced aplastic crisis in a family leading to the diagnosis of hereditary spherocytosis (HS) is a very rare condition being barely reported in the literature. We herein report a 4-year-old girl, her brother, and their mother who all presented with progressive pallor and jaundice after a febrile illness. The HPV B19 was diagnosed using polymerase chain reaction (PCR) ...

double pylorus (dp) is a rare condition characterized by the presence of two openings from the gastric antrum to the duodenal bulb, which may be congenital or acquired. herein, we describe a case of dp in a cirrhotic patient.

human parvovirus (hpv) b19 induced aplastic crisis in a family leading to the diagnosis of hereditary spherocytosis (hs) is a very rare condition being barely reported in the literature. we herein report a 4-year-old girl, her brother, and their mother who all presented with progressive pallor and jaundice after a febrile illness. the hpv b19 was diagnosed using polymerase chain reaction (pcr) ...

‎We present some existence and convergence results for a general class of nonexpansive mappings in partially ordered hyperbolic metric spaces‎. ‎We also give some examples to show the generality of the mappings considered herein.

Peeling skin syndrome (PSS) is a very rare keratinization disorder, characterized by spontaneous exfoliation of the stratum corneum. Herein, we report a case of non-inflammatory (type A) PSS.