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Article ; Online: Postconceptual Neonatal Dating by Transmastoid Ultrasound of Transcerebellar Diameter-Comparison to Crown Rump Length Measurement: A Proof of Concept Paper.

Aziz, Michael M / VanDillen, Michael / Combs, Abigail / Banker, Hiral / Cohen, Harris L

Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine

2023 Volume 43, Issue 1, Page(s) 65–70

Abstract: Objectives: Transcerebellar diameter (TCD) has been utilized prenatally as a tool to estimate gestational age (GA) when fetal growth aberrations are suspected. Traditionally, first trimester ultrasound (1TUS) has been the gold standard of dating a ... ...

Abstract	Objectives: Transcerebellar diameter (TCD) has been utilized prenatally as a tool to estimate gestational age (GA) when fetal growth aberrations are suspected. Traditionally, first trimester ultrasound (1TUS) has been the gold standard of dating a pregnancy in spontaneous pregnancies. We sought to determine if neonatal TCD measurement was as accurate as 1TUS in the estimation of postconceptual gestational age (PCGA). Methods: A retrospective cohort from a registry of high-quality transmastoid views of consecutive patients from July 2019 to November 2020, delivered from 24 to 34 weeks GA, and with a 1TUS were included. The reference PCGA was the sum of the GA at delivery by 1TUS and day of life. The PCGA by TCD was calculated from Chang et al for GA by TCD. Reference and experimental values were compared by correlation, agreement within 7 days, and Bland-Altman analysis. Results: Of the 154 individual patients in the registry of high-quality transmastoid views during the study period, 62 met inclusion and exclusion criteria. PCGA by 1TUS and TCD were highly correlated (r = 0.86, P < .001; κ = 47% agreement within 7 days of PCGA). The bias of PCGA by TCD was 4.6 days earlier than the PCGA by 1TUS (95% confidence interval of agreement: -29.2, 20). Conclusions: PCGA estimation by neonatal transmastoid TCD was highly correlated with that of 1TUS. It generally underestimates GA by 4.6 days. This relationship warrants further investigation to determine if this method of estimating PCGA in undated gestations is generalizable.
MeSH term(s)	Pregnancy ; Female ; Infant, Newborn ; Humans ; Crown-Rump Length ; Retrospective Studies ; Ultrasonography, Prenatal/methods ; Gestational Age ; Fetal Development ; Pregnancy Trimester, First
Language	English
Publishing date	2023-09-29
Publishing country	England
Document type	Journal Article
ZDB-ID	604829-8
ISSN	1550-9613 ; 0278-4297
ISSN (online)	1550-9613
ISSN	0278-4297
DOI	10.1002/jum.16336
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Erratum for: Wunderlich Syndrome: Comprehensive Review of Diagnosis and Management.

Shah, Jignesh N / Gandhi, Darshan / Prasad, Srinivasa R / Sandhu, Preet K / Banker, Hiral / Molina, Ryan / Khan, Muhammad Salman / Garg, Tushar / Katabathina, Venkata S

Radiographics : a review publication of the Radiological Society of North America, Inc

2023 Volume 43, Issue 7, Page(s) e239007

Language	English
Publishing date	2023-06-29
Publishing country	United States
Document type	Published Erratum
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.239007
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Article ; Online: Wunderlich Syndrome: Comprehensive Review of Diagnosis and Management.

Shah, Jignesh N / Gandhi, Darshan / Prasad, Srinivasa R / Sandhu, Preet K / Banker, Hiral / Molina, Ryan / Khan, Salman / Garg, Tushar / Katabathina, Venkata S

Radiographics : a review publication of the Radiological Society of North America, Inc

2023 Volume 43, Issue 6, Page(s) e220172

Abstract: Wunderlich syndrome (WS), which was named after Carl Wunderlich, is a rare clinical syndrome characterized by an acute onset of spontaneous renal hemorrhage into the subcapsular, perirenal, and/or pararenal spaces, without a history of antecedent trauma. ...

Abstract	Wunderlich syndrome (WS), which was named after Carl Wunderlich, is a rare clinical syndrome characterized by an acute onset of spontaneous renal hemorrhage into the subcapsular, perirenal, and/or pararenal spaces, without a history of antecedent trauma. Patients may present with a multitude of symptoms ranging from nonspecific flank or abdominal pain to serious manifestations such as hypovolemic shock. The classic symptom complex of flank pain, a flank mass, and hypovolemic shock referred to as the Lenk triad is seen in a small subset of patients. Renal neoplasms such as angiomyolipomas and clear cell renal cell carcinomas that display an increased proclivity for hemorrhage and rupture contribute to approximately 60%-65% of all cases of WS. A plethora of renal vascular diseases (aneurysms or pseudoaneurysms, arteriovenous malformations or fistulae, renal vein thrombosis, and vasculitis syndromes) account for 20%-30% of cases of WS. Rare causes of WS include renal infections, cystic diseases, calculi, kidney failure, and coagulation disorders. Cross-sectional imaging modalities, particularly multiphasic CT or MRI, are integral to the detection, localization, and characterization of the underlying causes and facilitate optimal management. However, large-volume hemorrhage at patient presentation may obscure underlying causes, particularly neoplasms. If the initial CT or MRI examination shows no contributary causes, a dedicated CT or MRI follow-up study may be warranted to establish the cause of WS. Renal arterial embolization is a useful, minimally invasive, therapeutic option in patients who present with acute or life-threatening hemorrhage and can help avoid emergency radical surgery. Accurate diagnosis of the underlying cause of WS is critical for optimal patient treatment in emergency and nonemergency clinical settings.
MeSH term(s)	Humans ; Follow-Up Studies ; Kidney Neoplasms/complications ; Kidney Neoplasms/diagnostic imaging ; Kidney Neoplasms/therapy ; Kidney/diagnostic imaging ; Hemorrhage/diagnostic imaging ; Hemorrhage/etiology ; Hemorrhage/therapy ; Shock
Language	English
Publishing date	2023-05-25
Publishing country	United States
Document type	Review ; Journal Article
ZDB-ID	603172-9
ISSN	1527-1323 ; 0271-5333
ISSN (online)	1527-1323
ISSN	0271-5333
DOI	10.1148/rg.220172
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Antenatal diagnosis of aneurysmal malformation of the vein of Galen.

Darji, Parth J / Gandhi, Viplav S / Banker, Hiral / Chaudhari, Hemang

BMJ case reports

2015 Volume 2015

Abstract: Vein of Galen malformation (VGAM) results from an aneurysmal aberration with an arteriovenous shunting of blood. Vein of Galen aneurysmal malformations are the most frequent arteriovenous malformations in infants and fetuses. The congenital malformation ... ...

Abstract	Vein of Galen malformation (VGAM) results from an aneurysmal aberration with an arteriovenous shunting of blood. Vein of Galen aneurysmal malformations are the most frequent arteriovenous malformations in infants and fetuses. The congenital malformation develops during weeks 6-11 of fetal development. Infants often die from high-output congestive heart failure.
MeSH term(s)	Adult ; Female ; Humans ; Intracranial Aneurysm/complications ; Intracranial Aneurysm/diagnostic imaging ; Pregnancy ; Ultrasonography, Prenatal ; Vein of Galen Malformations/complications ; Vein of Galen Malformations/diagnostic imaging
Language	English
Publishing date	2015-12-07
Publishing country	England
Document type	Case Reports ; Journal Article
ISSN	1757-790X
ISSN (online)	1757-790X
DOI	10.1136/bcr-2015-213785
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Splenic infarct with polysplenia syndrome and situs inversus.

Suthar, Tejas / Banker, Hiral / Shah, Mukesh / Thakkar, Gurudatt

BMJ case reports

2012 Volume 2012

Abstract: A rare case of spontaneous splenic infarction with polysplenia and situs inversus is presented. The diagnosis was made by ultrasound and confirmed by CT which showed multiple aberrant right-sided spleens with situs inversus and one of the spleen showing ... ...

Abstract	A rare case of spontaneous splenic infarction with polysplenia and situs inversus is presented. The diagnosis was made by ultrasound and confirmed by CT which showed multiple aberrant right-sided spleens with situs inversus and one of the spleen showing low attenuation areas representing infarct. Polysplenia syndrome is a rare entity associated with heterotaxy syndromes, congenital cyanotic heart diseases, billiary atresia, intestinal malrotation, immotile cilia syndrome, annular or short pancreas, preduodenal portal vein and vena caval anomalies.
MeSH term(s)	Child ; Diagnosis, Differential ; Diagnostic Imaging ; Heterotaxy Syndrome/diagnosis ; Heterotaxy Syndrome/surgery ; Humans ; Infarction/diagnosis ; Infarction/surgery ; Male ; Situs Inversus/diagnosis ; Situs Inversus/surgery ; Spleen/blood supply
Language	English
Publishing date	2012-08-14
Publishing country	England
Document type	Case Reports ; Journal Article
ISSN	1757-790X
ISSN (online)	1757-790X
DOI	10.1136/bcr.02.2012.5831
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Postmenopausal woman with vaginal mass: do not forget to see for uterine inversion.

Darji, Parth / Banker, Hiral / Gandhi, Viplav / Thakkar, Gurudatt

BMJ case reports

2012 Volume 2012

Abstract: Inversion of the uterus is a rare clinical problem. It is encountered as an obstetric emergency and is a diagnostic challenge in gynaecology. Non-puerperal inversion usually results from a tumour implanted on fundus of the uterus. Treatment depends on ... ...

Abstract	Inversion of the uterus is a rare clinical problem. It is encountered as an obstetric emergency and is a diagnostic challenge in gynaecology. Non-puerperal inversion usually results from a tumour implanted on fundus of the uterus. Treatment depends on the associated pathology and the stage of the inversion. A rare case of non-puerperal uterine inversion caused by a large fundal submucous fibroid in a 58-year-old woman resulting in lower abdominal pain and vaginal bleeding was reported. After removal of fibroid, reduction of the inversion was successful and then abdominal hysterectomy was performed.
MeSH term(s)	Abdominal Pain/etiology ; Female ; Humans ; Leiomyoma/complications ; Leiomyoma/diagnostic imaging ; Leiomyoma/surgery ; Middle Aged ; Postmenopause ; Ultrasonography ; Uterine Hemorrhage/etiology ; Uterine Inversion/etiology ; Uterine Inversion/surgery ; Uterine Neoplasms/complications ; Uterine Neoplasms/diagnostic imaging ; Uterine Neoplasms/surgery
Language	English
Publishing date	2012-08-13
Publishing country	England
Document type	Case Reports ; Journal Article
ISSN	1757-790X
ISSN (online)	1757-790X
DOI	10.1136/bcr-02-2012-5841
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Extra cranial invasive meningioma of fronto-temporo-parietal region of the skull vault.

Banker, Hiral / Shah, Dharita / Modi, Hardik / Salvi, Bharat

BMJ case reports

2012 Volume 2012

Abstract: Meningioma is the benign, unencapsulated neoplasm arising from meningo-epithelial arachnoid cells of cerebellopontine angle-internal auditory canal dura but extracranial meningiomas are very rare. In making the diagnosis of invasive meningioma, both ... ...

Abstract	Meningioma is the benign, unencapsulated neoplasm arising from meningo-epithelial arachnoid cells of cerebellopontine angle-internal auditory canal dura but extracranial meningiomas are very rare. In making the diagnosis of invasive meningioma, both changes of benign meningioma and invasive growth should be present. A case of the neglected invasive meningioma is described here which invaded approximately half of the fronto-temporo-parietal skull vault. The diagnosis was established and confirmed by the histopathology and immunohistochemistry, the cells were positive for epithelial membrane antigen, vimetin and progesterone receptors. The patient underwent surgical resection.
MeSH term(s)	Adult ; Diagnosis, Differential ; Frontal Bone/diagnostic imaging ; Frontal Bone/pathology ; Humans ; Male ; Meningeal Neoplasms/diagnosis ; Meningeal Neoplasms/diagnostic imaging ; Meningeal Neoplasms/pathology ; Meningioma/diagnosis ; Meningioma/diagnostic imaging ; Meningioma/pathology ; Parietal Bone/diagnostic imaging ; Parietal Bone/pathology ; Skull Neoplasms/diagnosis ; Skull Neoplasms/diagnostic imaging ; Skull Neoplasms/pathology ; Skull Neoplasms/secondary ; Temporal Bone/diagnostic imaging ; Temporal Bone/pathology ; Tomography, X-Ray Computed
Language	English
Publishing date	2012-02-25
Publishing country	England
Document type	Case Reports ; Journal Article
ISSN	1757-790X
ISSN (online)	1757-790X
DOI	10.1136/bcr.12.2011.5290
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Study of Neonatal Meningitis in Neonatal Septicemia- Can We Do Better?

Bijal Shah / Hiral shah / Deepa Banker / Anunaya katyar, Chandraprkash Gupta

National Journal of Medical Research, Vol 4, Iss 4, Pp 337-

2014 Volume 339

Abstract: Introduction: Neonatal meningitis is most of the time remains undetected in all neonatal septicemias as they may not show any signs and symptoms of meningitis. This study was therefore set out to look for the neonatal meningitis in early and late onset ... ...

Abstract	"Introduction: Neonatal meningitis is most of the time remains undetected in all neonatal septicemias as they may not show any signs and symptoms of meningitis. This study was therefore set out to look for the neonatal meningitis in early and late onset neonatal septicemic patients. Material and Method: This is a cross sectional observational study done in a tertiary care hospital from October 2012 to august 2013 in 155 neonates. Preformed questionnaires were used to note sign of meningitis in babies with early or late onset septicemias. In all groups CSF examination was done to rule out meningitis. Result: Out of 155,28(18%) were in grp A (with meningeal signs)and 126(82%) were inGroup B(without any signs). It was found that all the patients having meningeal signs were having positive CSF while 58 (48%) newborn were having a positive CSF instead of no meningeal signs( p value significant). Mortality was high 21% in group A and was significantly low10% in group B due to early diagnosis. Conclusion: CSF is a septic screen diagnostic test for late onset septicemia and should be done in all high risk early onset septicemias are proven facts still it is not done at many centers. " [Natl J Med Res 2014; 4(4.000): 337-339]
Keywords	neonatal ; meningitis ; septicemia ; Medicine (General) ; R5-920 ; Medicine ; R
Language	English
Publishing date	2014-12-01T00:00:00Z
Publisher	National Association for Medical Research
Document type	Article ; Online
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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Article ; Online: Recurrent ectopic pregnancy in a woman suffering from infertility due to male factor presented with heterotopic pregnancy.

Chaudhari, Hemang D / Gandhi, Viplav S / Banker, Hiral / Suri, Amar

BMJ case reports

2012 Volume 2012

Abstract: Heterotopic pregnancy is the simultaneous occurrence of intrauterine and extrauterine pregnancies. A 27-year-old third gravida with history of two ectopic pregnancies, presented with cramping pain in pelvis radiating to left side and bleeding from vagina. ...

Abstract	Heterotopic pregnancy is the simultaneous occurrence of intrauterine and extrauterine pregnancies. A 27-year-old third gravida with history of two ectopic pregnancies, presented with cramping pain in pelvis radiating to left side and bleeding from vagina. Ultrasonographic diagnosis of heterotopic pregnancy was put forward. Unfortunately intrauterine component of heterotopic pregnancy resulted in blighted ovum and linear salpingostomy was done for left-sided tubal pregnancy.
MeSH term(s)	Adult ; Female ; Humans ; Infertility, Male ; Male ; Pregnancy ; Pregnancy, Ectopic/diagnostic imaging ; Pregnancy, Ectopic/surgery ; Pregnancy, Heterotopic/diagnostic imaging ; Pregnancy, Heterotopic/surgery ; Recurrence ; Salpingostomy ; Ultrasonography
Language	English
Publishing date	2012-05-11
Publishing country	England
Document type	Case Reports ; Journal Article
ISSN	1757-790X
ISSN (online)	1757-790X
DOI	10.1136/bcr.02.2012.5784
Database	MEDical Literature Analysis and Retrieval System OnLINE

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Article ; Online: Spontaneous gastric perforation in 11-year-old boy with anorexia nervosa: rare presentation with right iliac fossa pain.

Darji, Parth / Gandhi, Viplav / Banker, Hiral / Chaudhari, Hemang D

publication RETRACTED

BMJ case reports

2012 Volume 2012

Abstract: Spontaneous gastric perforation is rare in children. It is usually associated with prematurity, foreign bodies and trauma. Anorexia nervosa (AN) can be an underlying condition although no cases are reported in the literature. We are reporting a rare case ...

Abstract	Spontaneous gastric perforation is rare in children. It is usually associated with prematurity, foreign bodies and trauma. Anorexia nervosa (AN) can be an underlying condition although no cases are reported in the literature. We are reporting a rare case of 11-year-old boy with AN who presented with right iliac fossa pain mimicking acute appendicitis. Intraoperative findings proved a gastric perforation. Pathophysiology of this condition in AN is poorly understood. Gastric smooth muscle atrophy and ischaemia can be the possible underlying mechanisms. The case discussed here highlights the fact that any abdominal pain in patients with underlying eating disorders should raise suspicion of perforation as diagnosis can be far more complicated.
MeSH term(s)	Abdominal Pain/etiology ; Anorexia Nervosa/complications ; Appendicitis/diagnosis ; Child ; Diagnosis, Differential ; Humans ; Male ; Rupture, Spontaneous/diagnosis ; Rupture, Spontaneous/etiology ; Rupture, Spontaneous/surgery ; Stomach Rupture/diagnosis ; Stomach Rupture/etiology ; Stomach Rupture/surgery
Language	English
Publishing date	2012-11-30
Publishing country	England
Document type	Case Reports ; Journal Article ; Retracted Publication
ISSN	1757-790X
ISSN (online)	1757-790X
DOI	10.1136/bcr-2012-006529
Database	MEDical Literature Analysis and Retrieval System OnLINE

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