Patient Demographics > Country of Treatment > Saudi Arabia
You are looking at 1 - 7 of 7 items
Ministry of National Guard – Health Affairs, Riyadh, Saudi Arabia
Search for other papers by Fahad Al-Juraibah in
Google Scholar
PubMed
Department of Paediatrics, Endocrine Division, Jeddah, Saudi Arabia
Search for other papers by Adnan Al Shaikh in
Google Scholar
PubMed
Search for other papers by Afaf Al-Sagheir in
Google Scholar
PubMed
Ministry of National Guard – Health Affairs, Riyadh, Saudi Arabia
Search for other papers by Amir Babiker in
Google Scholar
PubMed
Search for other papers by Asma Al Nuaimi in
Google Scholar
PubMed
Search for other papers by Ayed Al Enezi in
Google Scholar
PubMed
Search for other papers by George S Mikhail in
Google Scholar
PubMed
Search for other papers by Hassan A Mundi in
Google Scholar
PubMed
Search for other papers by Hubert K Penninckx in
Google Scholar
PubMed
Search for other papers by Huda Mustafa in
Google Scholar
PubMed
Search for other papers by Majid Al Ameri in
Google Scholar
PubMed
Ministry of National Guard – Health Affairs, Riyadh, Saudi Arabia
Search for other papers by Mohamed Al-Dubayee in
Google Scholar
PubMed
Search for other papers by Nadia S Ali in
Google Scholar
PubMed
Faculty of medicine, Sohag University, Egypt
Search for other papers by Nagla Fawzy in
Google Scholar
PubMed
Search for other papers by Sameer Al Shammari in
Google Scholar
PubMed
Search for other papers by Tarek Fiad in
Google Scholar
PubMed
Summary
X-linked hypophosphatemic rickets (XLH), the most prevalent form of inherited hypophosphatemic rickets, is caused by loss-of-function mutations in the gene encoding phosphate-regulating endopeptidase homolog, X-linked (PHEX). This case series presents 14 cases of XLH from Gulf Cooperation Council (GCC) countries. The patients’ medical history, biochemical and radiological investigative findings, as well as treatment responses and side effects from both conventional and burosumab therapy, are described. Cases were aged 2–40 years at diagnosis. There were two male cases and 12 female cases. All cases were treated with conventional therapy which resulted in a lack of improvement in or worsening of the clinical signs and symptoms of rickets or biochemical parameters. Side effects of conventional therapy included nausea, diarrhea, abdominal pain, nephrocalcinosis, and hyperparathyroidism, which affected the patients’ quality of life and adherence to treatment. In the 10 patients treated with burosumab, there was a marked improvement in the biochemical markers of rickets, with a mean increase in serum phosphate of +0.56 mmol/L and tubular maximum phosphate reabsorption (TmP) to glomerular filtration rate (GFR) ratio (TmP/GFR) of +0.39 mmol/L at 12 months compared to baseline. Furthermore, a mean decrease in serum alkaline phosphatase (ALP) of −80.80 IU/L and parathyroid hormone (PTH) of −63.61 pmol/L at 12 months compared to baseline was observed in these patients. Additionally, patients treated with burosumab reported reduced pain, muscle weakness, and fatigue as well as the ability to lead more physically active lives with no significant side effects of treatment.
Learning points
-
Conventional therapy resulted in a suboptimal response, with a lack of improvement of clinical signs and symptoms.
-
Side effects of conventional therapy included nausea, diarrhea, abdominal pain, nephrocalcinosis, and hyperparathyroidism, which affected the patients’ quality of life and adherence to treatment.
-
Burosumab demonstrated marked improvements in the biochemical markers of rickets, in addition to reducing pain, muscle weakness, and fatigue.
-
There were no significant side effects associated with burosumab therapy.
Search for other papers by Siham Hussein Subki in
Google Scholar
PubMed
Search for other papers by Raghad Wadea Mohammed Hussain in
Google Scholar
PubMed
Search for other papers by Abdulmoein Eid Al-Agha in
Google Scholar
PubMed
Summary
Congenital lipoid adrenal hyperplasia (CLAH) is characterized by a defect in the STAR protein-encoding gene that attenuates all steroidogenesis pathways. Herein, we present the first reported case in Saudi Arabia of a 46 XY, phenotypically female infant with an unfamiliar, darkened complexion compared to the family’s skin color. Based on the clinical and biochemical findings, CLAH was diagnosed and glucocorticoid replacement therapy was initiated. As a result, we suggest that pediatricians should always investigate the possibility of adrenal insufficiency when encountering unusual dark skin.
Learning points
-
Pediatricians should be prompted to rule out adrenal insufficiency in unexpectedly dark skin neonates.
-
In such patients, pediatricians should not wait until the neonate develops an adrenal crisis.
-
A low level of 17-hydroxyprogesterone does not always rule out the possibility of inherited adrenal gland disorders, and additional tests should be performed for early detection.
King Abdullah Specialized Children Hospital, Ministry of the National Guard Health Affairs, Riyadh, Saudi Arabia
King Abdullah International Medical Research Center, Riyadh, Saudi Arabia
Search for other papers by Amir Babiker in
Google Scholar
PubMed
Search for other papers by Wejdan Al Hamdan in
Google Scholar
PubMed
Search for other papers by Sondos Kinani in
Google Scholar
PubMed
King Abdullah Specialized Children Hospital, Ministry of the National Guard Health Affairs, Riyadh, Saudi Arabia
King Abdullah International Medical Research Center, Riyadh, Saudi Arabia
Search for other papers by Yasser Kazzaz in
Google Scholar
PubMed
Search for other papers by Abdelhadi Habeb in
Google Scholar
PubMed
King Abdullah Specialized Children Hospital, Ministry of the National Guard Health Affairs, Riyadh, Saudi Arabia
King Abdullah International Medical Research Center, Riyadh, Saudi Arabia
Search for other papers by Talal Al Harbi in
Google Scholar
PubMed
King Abdullah Specialized Children Hospital, Ministry of the National Guard Health Affairs, Riyadh, Saudi Arabia
King Abdullah International Medical Research Center, Riyadh, Saudi Arabia
Search for other papers by Mohammed Al Dubayee in
Google Scholar
PubMed
King Abdullah Specialized Children Hospital, Ministry of the National Guard Health Affairs, Riyadh, Saudi Arabia
King Abdullah International Medical Research Center, Riyadh, Saudi Arabia
Search for other papers by M Al Namshan in
Google Scholar
PubMed
King Abdullah Specialized Children Hospital, Ministry of the National Guard Health Affairs, Riyadh, Saudi Arabia
King Abdullah International Medical Research Center, Riyadh, Saudi Arabia
Search for other papers by Abdul Aleem Attasi in
Google Scholar
PubMed
Summary
The use of antihypertensive medications in patients with pheochromocytomas and paragangliomas (PCC/PG) is usually a challenge. We report a case of familial paraganglioma that was successfully treated by esmolol and other antihypertensive medications without associated perioperative complications. Our patient was an 11-year-old girl who presented with classic symptoms and signs of PCC/PG and a CT scan of the abdomen that showed a right-sided paravertebral mass. Her father was diagnosed with paraganglioma a few years ago. Prazosin had been started but she continued to experience uncontrolled paroxysms of blood pressure (BP). She was known to have asthma; hence, she developed serious bronchospasm with atenolol. She was, therefore, switched to esmolol that successfully controlled her BP in addition to prazosin and intermittent doses of hydralazine prior to laparoscopic surgery with no side effects of medications or postoperative complications. Esmolol could be a good alternative to routinely used beta-blockers in children with PCC/PG with labile hypertension and related symptoms in the pre and intra-operative periods. It is titrable, effective, and can be weaned rapidly helping to avoid postoperative complications. Further larger studies on the use of esmolol in children with PCC/PG are needed to confirm our observation.
Learning points
-
In addition to alpha-blockers, esmolol could be a good alternative for routinely used beta-blockers to control paroxysmal hypertension and tachycardia in the pre- and intra-operative periods.
-
Esmolol is titrable and an effective beta-blocker. It can be weaned rapidly helping to avoid postoperative complications in children with PCC/PG.
-
Children with PCC/PG and other comorbidity like asthma may particularly benefit from the use of esmolol due to no or less side effects on airway resistance and the advantage of rapid titration of the medication compared to other beta-blockers.
Search for other papers by Aishah Ekhzaimy in
Google Scholar
PubMed
Search for other papers by Afshan Masood in
Google Scholar
PubMed
Search for other papers by Seham Alzahrani in
Google Scholar
PubMed
Search for other papers by Waleed Al-Ghamdi in
Google Scholar
PubMed
Search for other papers by Daad Alotaibi in
Google Scholar
PubMed
Search for other papers by Muhammad Mujammami in
Google Scholar
PubMed
Summary
Central diabetes insipidus (CDI) and several endocrine disorders previously classified as idiopathic are now considered to be of an autoimmune etiology. Dermatomyositis (DM), a rare autoimmune condition characterized by inflammatory myopathy and skin rashes, is also known to affect the gastrointestinal, pulmonary, and rarely the cardiac systems and the joints. The association of CDI and DM is extremely rare. After an extensive literature search and to the best of our knowledge this is the first reported case in literature, we report the case of a 36-year-old male with a history of CDI, who presented to the hospital’s endocrine outpatient clinic for evaluation of a 3-week history of progressive facial rash accompanied by weakness and aching of the muscles.
Learning points:
-
Accurate biochemical diagnosis should always be followed by etiological investigation.
-
This clinical entity usually constitutes a therapeutic challenge, often requiring a multidisciplinary approach for optimal outcome.
-
Dermatomyositis is an important differential diagnosis in patients presenting with proximal muscle weakness.
-
Associated autoimmune conditions should be considered while evaluating patients with dermatomyositis.
-
Dermatomyositis can relapse at any stage, even following a very long period of remission.
-
Maintenance immunosuppressive therapy should be carefully considered in these patients.
Search for other papers by Ohoud Al Mohareb in
Google Scholar
PubMed
Search for other papers by Mussa H Al Malki in
Google Scholar
PubMed
Search for other papers by O Thomas Mueller in
Google Scholar
PubMed
Search for other papers by Imad Brema in
Google Scholar
PubMed
Summary
Resistance to thyroid hormone-beta (RTHbeta) is a rare inherited syndrome characterized by variable reduced tissue responsiveness to the intracellular action of triiodothyronine (T3), the active form of the thyroid hormone. The presentation of RTHbeta is quite variable and mutations in the thyroid hormone receptor beta (THR-B) gene have been detected in up to 90% of patients. The proband was a 34-year-old Jordanian male who presented with intermittent palpitations. His thyroid function tests (TFTs) showed a discordant profile with high free T4 (FT4) at 45.7 pmol/L (normal: 12–22), high free T3 (FT3) at 11.8 pmol/L (normal: 3.1–6.8) and inappropriately normal TSH at 3.19 mIU/L (normal: 0.27–4.2). Work up has confirmed normal alpha subunit of TSH of 0.1 ng/mL (normal <0.5) and pituitary MRI showed no evidence of a pituitary adenoma; however, there was an interesting coincidental finding of partially empty sella. RTHbeta was suspected and genetic testing confirmed a known mutation in the THR-B gene, where a heterozygous A to G base change substitutes valine for methionine at codon 310. Screening the immediate family revealed that the eldest son (5 years old) also has discordant thyroid function profile consistent with RTHbeta and genetic testing confirmed the same M310V mutation that his father harbored. Moreover, the 5-year-old son had hyperactivity, impulsivity and aggressive behavior consistent with attention deficit hyperactivity disorder (ADHD). This case demonstrates an unusual co-existence of RTHbeta and partially empty sella in the same patient which, to our knowledge, has not been reported before.
Learning points:
-
We report the coincidental occurrence of RTHbeta and a partially empty sella in the same patient that has not been previously reported.
-
TFTs should be done in all children who present with symptoms suggestive of ADHD as RTHbeta is a common finding in these children.
-
The management of children with ADHD and RTHbeta could be challenging for both pediatricians and parents and the administration of T3 with close monitoring may be helpful in some cases.
-
Incidental pituitary abnormalities do exist in patients with RTHbeta, although extremely rare, and should be evaluated thoroughly and separately.
Search for other papers by Wael M Almistehi in
Google Scholar
PubMed
King Fahad Medical City, College of Medicine, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia
Search for other papers by Mussa H Almalki in
Google Scholar
PubMed
Summary
Giant prolactinomas are a rare entity; during pregnancy, the risk for complications associated with these tumors is higher. Here, we report a case of a young woman who had an invasive, giant prolactinoma post resection with residual disease who became pregnant. This patient was treated with cabergoline to prevent tumor expansion in pregnancy, resulting in the uneventful delivery of a healthy baby boy.
Learning points:
-
Giant prolactinoma can cause both diagnostic and therapeutic challenges given their atypical presentation.
-
Accurate diagnosis is paramount to avoid unnecessary surgical intervention or pituitary irradiation.
-
This case demonstrates the effectiveness and safety of CAB therapy during pregnancy.
Search for other papers by Noman Ahmad in
Google Scholar
PubMed
Search for other papers by Abdulmonem Mohammed Almutawa in
Google Scholar
PubMed
Search for other papers by Mohamed Ziyad Abubacker in
Google Scholar
PubMed
Search for other papers by Hossam Ahmed Elzeftawy in
Google Scholar
PubMed
Search for other papers by Osama Abdullah Bawazir in
Google Scholar
PubMed
Summary
An insulinoma is a rare tumour with an incidence of four cases per million per year in adults. The incidence in children is not established. There is limited literature available in children with insulinoma, and only one case is reported in association with Down’s syndrome in adults. Insulinoma diagnosis is frequently missed in adults as well as in children. The Whipple triad is the most striking feature although it has limited application in young children. Hypoglycaemia with elevated insulin, C-peptide and absent ketones is highly suggestive of hyperinsulinism. We present a case of 10-year-old boy with Down’s syndrome with recurrent insulinoma. He was initially misdiagnosed as having an adrenal insufficiency and developed cushingoid features and obesity secondary to hydrocortisone treatment and excessive sugar intake. The tumour was successfully localised in the head of the pancreas with an MRI and octreotide scan on first presentation. Medical treatment with diazoxide and octreotide could not achieve normal blood glucose levels. The insulinoma was laparoscopically enucleated and pathological examination confirmed a neuroendocrine tumour. Subsequently, he had complete resolution of symptoms. He had a recurrence after 2 years with frequent episodes of hypoglycaemia. The biochemical workup was suggestive of hyperinsulinism. MRI and PET scan confirmed the recurrence at the same site (head of the pancreas). He had an open laparotomy for insulinoma resection. The pathology was consistent with benign insulinoma, and subsequently, he had complete resolution of symptoms.
Learning points:
-
Insulinoma is a very rare tumour in children; it should be considered in the differential diagnosis of hypoglycaemia with absent ketones.
-
Refractory neurological symptoms like seizure, migraine, mood changes and regression of learning abilities should suggest evaluation for hypoglycaemia.
-
MRI with contrast and PET scan would localise the majority of pancreatic beta islet cell lesions.
-
Medical treatment with diazoxide, octreotide and the addition of corn starch in feeds is not curative but can be supportive to maintain normoglycemia until the surgical resection.
-
Surgical resection is the only curative treatment. The surgical procedure of choice (laparoscopic/open laparotomy) depends on local expertise, preoperative localisation, tumour size and number.
-
Surgical treatment results in complete resolution of symptoms, but all cases should be closely followed up to monitor for recurrence. The recurrence rate is four times higher in MEN1 cases.
