• Nenhum resultado encontrado

Sao Paulo Med. J. vol.135 número2

N/A
N/A
Protected

Academic year: 2018

Share "Sao Paulo Med. J. vol.135 número2"

Copied!
2
0
0

Texto

(1)

190 Sao Paulo Med J. 2017; 135(2):190-1

LETTER TO THE EDITOR

DOI: 10.1590/1516-3180.2016.0354020117

Boerhaave syndrome and black esophagus

Síndrome de Boerhaave e esôfago preto

Grigoriy Emil Gurvits

I

New York University School of Medicine/Langone Medical Center, New York, United States

Dear Editor,

It was with great interest that I read an article by Dr. Dinic and colleagues on Boerhaave syndrome in the latest issue of your journal.1 hey describe a rare case of spontaneous

esophageal perforation in the setting of hematemesis in association with duodenal ulcer and black esophagus.

Boerhaave syndrome is an unusual entity in clinical medicine that was historically described by classical physical examination indings of the Mackler triad (vomiting, chest pain and sub-cutaneous emphysema), Hamman’s mediastinal crepitus with heartbeat and pneumomediasti-num on X-ray imaging. Computed tomography scans showing Gastrograin extravasation are diagnostic on call to the operating room.2 Patients typically appear tachypneic and acutely ill.

he case of esophageal perforation presented by Dinic et al. is intriguing for several reasons, primarily because of the presence of a rare inding of distal black esophagus on postmortem examination. Black esophagus or acute esophageal necrosis is a syndrome that is classically characterized by a distal esophagus with circumferential black appearance of varying proxi-mal extent. It presents clinically with gastrointestinal hemorrhage and is oten associated with duodenal ulcer disease.3-5 he patient’s clinical history and a four day prodrome may be a clue

to the development of black esophagus.

It is true that profound retching with a sudden rise in intraesophageal pressure against a closed cricopharyngeus may result in spontaneous distal esophageal perforation, as seen in Boerhaave syndrome. On the other hand, blind passage of the nasogastric tube in the setting of a necrotic esophagus would potentially cause a longitudinal tear of similar appearance at the weak point just above the gastroesophageal junction. In fact, such a procedure should be avoided.4 It is also

conceivable that repeated vomiting in a patient with black esophagus may result in Boerhaave syndrome. If so, this would be the irst such occurrence described in the literature.

It is diicult to retrospectively point out the correct underlying diagnosis in this unfor-tunate case, but the possibility of an iatrogenic esophageal tear should be considered in this patient with concurrent inding of black esophagus.

IMD, FACP, FACG. Clinical Associate Professor,

(2)

Boerhaave syndrome and black esophagus | LETTER TO THE EDITOR

Sao Paulo Med J. 2017; 135(2):190-1 191

REFERENCES

1. Dinic BR, Ilic G, Rajkovic ST, Stoimenov TJ. Boerhaave syndrome - case

report. Sao Paulo Med J. 2016;12:0. [Epub ahead of print]

2. Gurvits GE. Education and imaging. Gastrointestinal: “Walk in the snow”:

Boerhaave syndrome. J Gastroenterol Hepatol. 2011;26(1):207.

3. Gurvits GE, Cherian K, Shami MN, et al. Black esophagus: new insights and

multicenter international experience in 2014. Dig Dis Sci. 2015;60(2):444-53.

4. Gurvits GE. Black esophagus: acute esophageal necrosis syndrome. World

J Gastroenterol. 2010;16(26):3219-25.

5. Gurvits GE, Shapsis A, Lau N, Gualtieri N, Robilotti JG. Acute esophageal

necrosis: a rare syndrome. J Gastroenterol. 2007;42(1):29-38.

Sources of funding: None

Conlict of interest: None

Date of irst submission: December 27, 2016

Last received: December 27, 2016

Accepted: January 2, 2017

Address for correspondence:

Department of Medicine, Division of Gastroenterology,

New York University School of Medicine/Langone Medical Center,

240 East 38th Street, New York, NY 10016, USA

Tel. +1-212-263-3095

Fax. +1-212-263-3096

E-mail: g_g@hotmail.com

RESPONSE TO LETTER TO THE EDITOR

Biljana Radovanovic Dinic

I

, Goran Ilic

II

, Snezana Tesic

Rajkovic

III

, Tatjana Jevtovic Stoimenov

IV

IMD. Associate Professor and Attending Physician, Medical School, University of

Niš, and Gastroenterology and Hepatology Clinic, Niš Clinical Center, Niš, Serbia.

IIMD. Associate Professor, Medical School, University of Niš, and Institute of

Forensic Medicine, Niš, Serbia.

IIIMD. Attending Physician, Gastroenterology and Hepatology Clinic, Niš

Clinical Center, Niš, Serbia.

IVMD. Associate Professor, Medical School, University of Niš, and Institute of

Biochemistry, Niš, Serbia.

Dear Sir,

I am glad that our work has sparked your interest. he study1

presents a case of a patient with spontaneous rupture of the esoph-agus caused by vomiting. In Figure 2, we presented the esophesoph-agus with its surface covered with blood (not washed). he wall of the esophagus was not necrotized (shown histopathologically), and it was not a black esophagus.2,3 Setting the nasogastric tube in this

case was risky; however, it was necessary in order to evacuate the heavy liquid content of the stomach (detected on abdominal ultra-sound), as well as to perform esophagogastroduodenoscopy (EGD). he patient had the same symptoms before placing the probe and

ater removing it (before EGD), and so we ruled out the possibil-ity that she might have caused the rupture herself.

REFERENCES

1. Dinic BR, Ilic G, Rajkovic ST, Stoimenov TJ. Boerhaave syndrome - case

report. Sao Paulo Med J. 2016;12:0. [Epub ahead of print]

2. Kimura Y, Seno H, Yamashita Y. A case of acute necrotizing esophagitis.

Gastrointest Endosc. 2014;80(3):525-6.

3. Gurvits GE, Cherian K, Shami MN, et al. Black esophagus: new insights and

Referências

Documentos relacionados

We included RCTs or quasi-RCTs that compared reiki therapy and prayer meditation with the usual care among pregnant women undergoing cesarean section, including any of the

Clinical Research Center, University Hospital, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo (SP),

Helicobacter pylori infection among children up to ive years of age in an urban indigenous community of Guarani ethnicity in the city of São Paulo,

he parenchymal form, which is generally the most common type, usually does not require neurosurgical intervention, unlike cases in which the disease has an extraparenchymal

The aim of this study was to analyze and compare the association between the Gini coeicient (which is used to measure inequality) and suicide death rates over a 14-year

RESULTS: Consumption of saturated fatty acids (SFAs) was related to postprandial upregulation of genes associated with pro-inlammatory pathways in peripheral blood mononuclear

Some studies on interactions between probiotics and gene expres- sion have suggested that type 2 diabetes in rats is ameliorated through mRNA upregulation of glucose

CASE REPORT: Here, we describe a case of APL with high white blood cell counts in blood tests and hypogranular variant morphology in bone marrow, together with fms-like