scholarly journals Bohn’s Nodule: A Rare Case in a 7-month-old Male Infant

2021 ◽  
Keyword(s):  
Rare Case ◽  
Male Infant

scholarly journals Neonatal Abdominal Hemangiomatosis: Propranolol beyond Infantile Hemangioma

2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Siu Ying Angel Nip ◽  
Kam Lun Hon ◽  
Wing Kwan Alex Leung ◽  
Alexander K. C. Leung ◽  
Paul C. L. Choi
Keyword(s):  
Cardiac Failure ◽  
Rare Case ◽  
Male Infant ◽  
Infantile Hemangioma ◽  
Vascular Tumor ◽  
Life Threatening ◽  
Cutaneous Hemangioma ◽  
Benign Course ◽  
Hepatic Hemangiomas ◽  
High Output

Hemangioma is the most common vascular tumor of infancy; presentation is often as cutaneous infantile hemangioma (IH). Cutaneous hemangioma is a clinical diagnosis. Most IHs follow a benign course, with complete involution without treatment in the majority of cases. Visceral hemangioma often involves the liver and manifests as a life-threatening disorder. Hepatic hemangiomas may be associated with high output cardiac failure, coagulopathy, and hepatomegaly which generally develop between 1 and 16 weeks of age. Mortality has been reportedly high without treatment. We report a rare case of a male infant with neonatal hemangiomatosis with diffuse peritoneal involvement, which mimicked a malignant-looking tumor on imaging, and discuss therapeutic options and efficacy. Propranolol is efficacious for IH but generally not useful for other forms of vascular hemangiomas, tumors, and malformations. In our case of neonatal peritoneal hemangiomatosis, propranolol appears to have halted the growth and possibly expedite the involution of the hemangiomatosis without other treatments.

scholarly journals Salmonella Meningitis in a Two Months Infant from Odisha, India: A Rare Case Report

2021 ◽  
Vol 8 (2) ◽  
pp. 153-155
Author(s):  
C. P. Khuntia ◽  
S. K. Kar ◽  
N. Mohanty ◽  
H. K. Khuntia ◽  
B. Dwibedi
Keyword(s):  
Cerebrospinal Fluid ◽  
Rare Case ◽  
Young Infant ◽  
Male Infant ◽  
Salmonella Typhi ◽  
Enteric Infection ◽  
Risk Of Mortality ◽  
Rare Case Report ◽  
Salmonella Meningitis ◽  
Breast Fed

Salmonella meningitis is a disease with high mortality in infants though incidence is rare. This article reports a case of Salmonella meningitis in a two months male infant, who presented with high fever, convulsion and difficulty in breathing. Salmonella typhi was isolated from cerebrospinal fluid (CSF), that showed resistance to Cephalosporins, Fluroquinoles, Macrolides and Aminoglycosides but susceptiblity to Chloramphenicol and Cotrimaxozole. This case was admitted on fourth day of onset of illness and treated with parenteral Vancomycin and Ceftriaxone to cover both gram positive and negative bacterial agents of bacterial meningitis in a young infant, but succumbed to death on ninth day of illness. This indicated importance of S. typhi as a possible bacterial etiology and a great concern on resistance to the normally chosen antibiotics. An early suspicion can be suggested to reduce the risk of mortality. Environmental hygiene and household cleanliness practices also warrants attention, which were identified as possible risks for enteric infection in spite the baby was absolutely breast fed.

scholarly journals A Rare Case of Sacrococcygeal Teratoma With Medullar Invasion

2020 ◽  
Vol 6 (4) ◽  
pp. 229-232
Author(s):  
Najoua Aballa ◽  
◽  
Houssine Ghannane ◽  
Mohamed Oulad Saiad ◽  
◽  
...  
Keyword(s):  
Rare Case ◽  
Male Infant ◽  
Surgical Excision ◽  
Sacrococcygeal Teratoma ◽  
Tissue Mass ◽  
Pelvic Magnetic Resonance Imaging ◽  
Risk Of Malignancy ◽  
History Of ◽  
Magnetic Resonance Imaging Mri ◽  
High Level

Background and Importance: Sacrococcygeal Teratoma (SCT) with medular invasion is rare. Case Presentation: We report a case of an 11-month male infant, with no prenatal history of any abnormality, presenting since birth, a mass in the buttock extended to retrorectum associated with a right side hypotonic limb and monoplegia. Medullar and abdominal pelvic Magnetic Resonance Imaging (MRI) showed a sacrococcygeal tissue mass and intradural lumbosacral invasion with a high level of alpha-fetoprotein. Surgical excision was done successfully with an uneventful follow-up. Conclusion: Despite of the intradural invasion, those SCT are in major cases mature and present low risk of malignancy or recurrence.

scholarly journals Acquired colonic atresia in a 4-month old term male infant: a rare case report

2017 ◽  
Vol 4 (2) ◽  
pp. 669
Author(s):  
Kamal Nain Rattan ◽  
Gurupriya J. ◽  
Shruti Bansal ◽  
Rohit Kapoor ◽  
Roomi Yadav
Keyword(s):  
Case Report ◽  
Necrotizing Enterocolitis ◽  
Rare Case ◽  
Male Infant ◽  
Abdominal Distension ◽  
Exploratory Laparotomy ◽  
Inflammatory Mass ◽  
Colonic Atresia ◽  
Rare Case Report ◽  
History Of

Acquired colonic atresias are very rare but, are known in association with necrotizing enterocolitis. We report a case of a 4-month term male infant with recurrent episodes of abdominal distension, bilious vomiting and constipation off and on, without the history of necrotizing enterocolitis. Exploratory laparotomy was performed, an inflammatory mass with multiple dense interloop adhesions were found in the mid-transverse colon. These adhesions were lysed to identify the proximal dilated and distal blind end of the colon.  Rest of the gut was normal.  This case is unique for the fact that, it is a case of acquired colonic atresia without history of necrotizing enterocolitis, unlike other reported cases of acquired colonic atresia.

Concomitant Congenital Horner and Harlequin Syndromes: Case Report and Review of Literature

2020 ◽  
Author(s):  
Ayman G. Elnahry ◽  
Aisha A. Gamal Eldin ◽  
Aya G. Elnahry ◽  
Gehad A. Elnahry
Keyword(s):  
Case Report ◽  
Autonomic Dysfunction ◽  
Rare Case ◽  
Rare Condition ◽  
Male Infant ◽  
The Other ◽  
Review Of Literature ◽  
Harlequin Syndrome ◽  
Congenital Condition ◽  
Autonomic Disturbances

AbstractHarlequin syndrome is a condition characterized by autonomic dysfunction leading to hemifacial flushing on one side with pallor and impaired sweating on the other side. It is a rare condition that can be both congenital and acquired, with congenital cases being rarer, comprising ∼6% of all Harlequin syndrome cases. Harlequin syndrome is usually associated with other autonomic disturbances including Horner syndrome especially when presenting as a congenital condition. We reported the findings of a rare case of concomitant congenital Horner and Harlequin syndromes in an otherwise healthy 4-month-old male infant patient and provided a review of the current literature.

scholarly journals A RARE CASE OF COMPLETE ECTOPIA CORDIS WITH COMPLEX CONGENITAL CARDIAC ANOMALIES

2020 ◽  
pp. 77-79
Author(s):  
Megha M Sheth ◽  
Yashpal R Rana ◽  
Meet Patel ◽  
Dinesh Patel ◽  
Samir Patel ◽  
...  
Keyword(s):  
Rare Case ◽  
Tertiary Care ◽  
Male Infant ◽  
Rare Form ◽  
Ectopia Cordis ◽  
Apgar Scores ◽  
Cardiac Anomalies ◽  
Peripheral Hospital ◽  
Congenital Cardiac Anomalies ◽  
Rare Case Report

Ectopia cordis is a very rare form of congenital malformation in which the heart is located outside the thorax, partially or totally. This abnormally located heart may be found in different anatomical locations, such as thoracic, abdominal, thoraco-abdominal, cervical or cervicothoracic. In majority, the heart projects outside the chest through a breach in sternum. This unique rare case report presents a male infant born at a peripheral hospital which was later referred to out tertiary care cardiac research institute. In our case thoracic ectopia was associated with complex cardiac anomalies. The baby had good APGAR scores at birth. The baby died 10 days after birth as a result of cardiac failure and septicaemia.

Oesophageal foreign body and a double aortic arch: rare dual pathology

2009 ◽  
Vol 123 (12) ◽  
pp. 1404-1406 ◽  
Author(s):  
T E O'Connor ◽  
T Cooney
Keyword(s):  
Foreign Body ◽  
Aortic Arch ◽  
Respiratory Symptoms ◽  
Rare Case ◽  
Male Infant ◽  
Double Aortic Arch ◽  
Review Of The Literature ◽  
Tracheal Compression ◽  
Vascular Rings ◽  
Dual Pathology

AbstractObjective:We report the rare case of an oesophageal foreign body which lodged above the site of oesophageal compression by a double aortic arch.Methods:Case report and a review of the literature surrounding the classification, embryology, diagnosis and management of vascular rings and slings.Results:An eight-month-old male infant presented with symptoms of tracheal compression following ingestion of an oesophageal foreign body. Following removal of the oesophageal foreign body, the infant's symptoms improved initially. However, subsequent recurrence of respiratory symptoms lead to a repeat bronchoscopy and the diagnosis of a coexisting double aortic arch, causing tracheal and oesophageal compression.Conclusion:To our knowledge, this is only the second reported case of a double aortic arch being diagnosed in a patient following removal of an oesophageal foreign body.

scholarly journals Amyand’s hernia in infant: A rare entity

2010 ◽  
Vol 7 (2) ◽  
pp. 143-144
Author(s):  
VD Upadhyaya ◽  
V Kumar ◽  
P Srivastava ◽  
AN Gangopadhyaya
Keyword(s):  
Medical Journal ◽  
Inguinal Hernia ◽  
Key Words ◽  
Rare Case ◽  
English Literature ◽  
Male Infant ◽  
Vermiform Appendix ◽  
Amyand’S Hernia ◽  
Rare Entity ◽  
Inguinal Herniotomy

The chance of vermiform appendix lying with in a hernial sac is 1% or less and is known as Amyand's hernia and it is very rare in infant and neonate. Till date, only twenty cases had been reported in English literature. We are reporting a rare case of Amyand's hernia where appendix was present in right inguinal sac of non-obstructed inguinal hernia in a seven month old male infant during operation. The appendectomy was done along with right inguinal herniotomy. In most of the reported cases, appendix was inflamed or perforated, expect in one case where appendix was not inflamed but patient presented with inguinal hernia. This case is reported because of the rarity of Amyand's hernia in infant, the appendix was not inflamed, hernia was not obstructed, and whether in such types of cases appendix should be preserved or not. Key words: Amyand's hernia; infant; appendectomy DOI: 10.3126/kumj.v7i2.2708 Kathmandu University Medical Journal (2009) Vol.7, No.2 Issue 26, 143-144

scholarly journals A Rare Case of a Congenital Nasopharyngeal Ganglioglioma With Dyspnea in a 1-Month-Old Male Infant: A Case Report

2021 ◽  
Vol 9 ◽  
Author(s):  
He Zhao ◽  
Zhiwei Cao ◽  
Zhaowei Gu
Keyword(s):  
Rare Case ◽  
Nasal Congestion ◽  
Tumor Resection ◽  
Male Infant ◽  
Resonance Imaging ◽  
Complete Tumor Resection ◽  
Plasma Technique ◽  
Case Summary ◽  
The Central Nervous System ◽  
Complete Tumor

Background: A ganglioglioma (GG), a tumor with both neuronal and astrocytic components, rarely occurs outside the central nervous system.Case Summary: We present the first reported case of a 1-month-old male with a congenital nasopharyngeal GG, nasal congestion, and dyspnea; we include the operative video. Magnetic resonance imaging was used to explore whether the tumor communicated with the intracranial space. We used an endoscopic plasma technique to ensure complete tumor resection. This afforded a good visual field, endoscopic magnification, and good hemostasis.Conclusions: We report a rare case of a nasopharyngeal GG triggering nasal congestion and dyspnea in a 1-month-old male, and report our experience with the treatment of nasopharyngeal GG and similar diseases.

Sign in / Sign up

Export Citation Format

Share Document