Keywords
mucormycosis reconstruction - zygomycosis reconstruction - mucormycosis flap
Mucormycosis is a rare (0.43 to 1.7 cases per million per year)[1] invasive fungal infection caused by various opportunistic fungi of the Mucoraceae
family. Eighty percent of these infections are caused by Rhizopus, Mucor, and Lichtheimia and usually affect poorly controlled diabetic patients (36%), followed by patients
with malignancy (17%), and solid organ transplantation (7%) among others.[2] However, in developing countries, diabetes incidence could be much more common (>
80%) than found in other parts of the world.
Mucormycosis was considered fatal until the 1960's when amphotericin was introduced
as a treatment. Thirty years later, encapsulated liposomes enhanced intracellular
amphotericin delivery, thus decreasing the renal toxicity and increasing the therapeutic
index by more than 20-fold.[3] Today, the reported mortality is 50 to 90% depending on the disease form.[2]
In this study, we present 16 patients who underwent reconstruction after head and
neck mucormycosis in addition to our personal experience with four immediate and one
late reconstruction.
Methods
Our reported case series was conducted as a retrospective study at Hospital Regional
de Alta Especialidad de Ixtapaluca, Estado de México, Mexico. Five patients, consisting
of three males and two females with a mean age of 39 years (range, 17–51 years) who
presented with infections between June 2017 and June 2018 ([Table 1]) are described. The etiological cause of the mucormycosis was diabetes mellitus
in four patients and trauma in one; all of them underwent reconstruction using free
(four-fifths) or pedicle (one-fifth) flaps. The study was retrospective and, therefore,
did not require approval from the ethics committee. The medical charts were reviewed
to obtain the following data: (1) age, (2) sex, (3) localization, (4) comorbidities,
(5) medical treatment, (6) surgical resection, (7) flap type, and (8) time from debridement
surgery to reconstruction.
Table 1
Present case series of reconstruction in head and neck mucormycosis
Case
|
Sex/age (y)
|
Etiology
|
Surgical resection and reconstruction
|
Outcome
|
1
|
F/41
|
DM2, ARF, MOF
|
Left orbital exenteration, resection of the submandibular gland, left facial muscles.
Reconstructed with a free 22 cm × 16 cm ALT flap, anastomosed to the superior thyroid
artery
|
Flap without complications, patient deceased after 10 days[a]
|
2
|
M/42
|
Trauma
|
Right orbital exenteration and frontotemporal craniectomy. Reconstructed with a frontal
flap and a second stage methyl methacrylate cranial prosthesis
|
Flap survival and asymptomatic. With a 1-year follow-up
|
3
|
M/51
|
Smoker, DM2, ARF, SAH
|
Left hemifacial skin resection, left orbital exenteration and total maxillectomy.
Reconstructed with a free 18 cm × 12 cm ALT flap, anastomosed to the facial artery
|
Flap survival and asymptomatic. With 5 months of follow-up
|
4
|
F/17
|
DM2
|
Right orbital exenteration + left total maxillectomy. Reconstructed with a free 12
cm × 7 cm MSAP flap, anastomosed to the facial artery[
b
]
|
Flap survival and asymptomatic. With 3 months of follow-up
|
5
|
M/46
|
DM2
|
Left orbital exenteration, left total and right infrastructure maxillectomy, partial
ethmoidectomy and sphenoidectomy. Reconstructed with a free chimeric 20 cm × 10 cm
ALT-VL flap, anastomosed to the temporal artery
|
Flap survival after 2 weeks, no follow-up[
c
]
|
Abbreviations: ALT, anterolateral thigh; ARF, acute renal failure; DM2, diabetes mellitus
type 2; F, female; M, male; MOF, multi organic failure; MSAP, medial sural artery
perforator; SAH, systemic arterial hypertension; VL, vastus lateralis.
a Deceased secondary to intra-hospitalary pneumonia.
b Reconstructed 5 weeks after surgery due to presenting hypha invasion in the vein
wall ([Fig. 1]).
c Patient was discharged by his own will and did not presented for follow-up.
Operative Technique
Once an infection is diagnosed, parenteral antifungal therapy was initiated with liposomal
amphotericin B (L-AmB), and a contrast computed tomography (CT) scan was requested
for surgical planning. The volume and size needed for the reconstruction were calculated
to choose an adequate flap for reconstruction. The flap type was selected depending
on the CT scan or the magnetic resonance image (MRI) findings and by calculating the
possible volume and flap size. If more volume was required, a chimeric flap was planned.
The resection was assessed by a multidisciplinary team (oncological, maxillofacial,
and plastic surgeons). A two-team approach was used thus reducing the time of surgery
and wound contamination in the donor area. The skin and soft tissue were resected
with a 1-cm margin of macroscopic healthy tissue in addition to a complete resection
from all of the affected bone.
Meanwhile, flap elevation started by raising one of the flap's borders to find the
primary perforator and start of the pedicle dissection until the desired length was
reached. All resected specimens were then sent to the pathologist for positive border
evaluation. The samples were examined after hematoxylin and eosin staining (20–30 minutes)
for rapid hyphae evaluation ([Fig. 1]). The definitive biopsies were evaluated after staining with Grocott's methenamine
silver. After the intraoperative analysis, with no apparent affected tissue left,
we selected the recipient vessels, while considering flap colocation, and pedicle
length. After dissection, we sent 1 to 2 mm of the distal portion from the recipient
artery and vein for hyphae analysis according to the previously described procedure.
When no signs of invasion were confirmed and all apparent macro and microscopically
affected tissues were debrided, the pedicle was freed and anastomosis performed. After
surgery, all patients were admitted to the intensive care unit for surveillance. If
the patient had a satisfactory response after at least 3 weeks of L-AmB, the parenteral
antifungal was switched to oral posaconazole.
Fig. 1 A transverse cut of the temporal vein, treated with hematoxylin and eosin stain,
thus presenting extensive wall fibrosis. The presence of broken hyphae invasion in
the vein wall can be observed (black arrow).
Search Strategy
The search was done using MEDLINE, Google Scholar, PubMed Central, and Embase databases
using the following English language keywords combined with Boolean logical operators:
(“Mucormycosis Reconstruction” or “Zygomycosis Reconstruction” or “Mucormycosis Flap”
or “Rhino-Orbital infection Reconstruction” [title/abstract/medical subject headings
(MeSH) terms]). There were no limits on the search; only articles written in English
were selected. Duplicates occurring in the different databases were removed. From
the search, publications were ordered by date (from December 1, 1988 to June 1, 2018).
A total of 154 articles were chosen by their title (containing the above-mentioned
keywords), and 134 articles were excluded based on the information in the abstract
(by not being reconstruction cases in mucormycosis patients) and from those remaining
20 articles, five publications were excluded due to the lack of head and neck reconstruction.
One other publication was excluded for insufficient patient information. The references
of the selected articles were also examined for possible additional relevant articles.
In summary, a total of 16 patients from 14 different publications were collected ([Table 2]). Studies identified through the electronic and manual searches were listed with
key information using Microsoft Excel 2011 (Microsoft Corp., Redmond, WA).
Table 2
All published cases of reconstruction in head and neck mucormycosis
Author (year)
|
Age (y)/sex
|
Etiology
|
Surgical treatment
|
Type of reconstruction
|
Time of reconstruction
|
Alleyne et al (1999)[4]
|
24/M
|
DM2
|
Three interventions: right total maxillectomy, right orbital exenteration, and dissection
of the trigeminal nerve
|
Temporalis muscle flap
|
Late
|
Lari et al (2002)[5]
|
35/F
|
DM2
|
Left orbital exenteration and left external ethmoidectomy
|
Galeal frontalis–pericranial flap
|
3 mo
|
Shand et al (2004)[15]
|
27/M
|
Trauma
|
Eight interventions: debridement, left orbital exenteration, left suprastructure maxillectomy
|
RFFF
|
52 d
|
Tidwell et al (2005)[6]
|
1.5/F
|
Trauma
|
Four interventions: skin and soft tissue debridements
|
Pre-expanded cervicofacial flap
|
2 wk
|
Adler et al (2008)[8]
|
45/M
|
DM2
|
Three interventions: Left orbital exenteration, left total maxillectomy, sphenoidectomy,
and ethmoidectomy
|
LFCP chimeric free flap with VL
|
Immediate
|
41/M
|
Trauma
|
Scalp and a 10 × 10 cm cranial bone resection
|
LDFF + 7th rib
|
Early
|
Odessey et al (2008)[13]
|
64/M
|
DM2
|
Right subtotal maxillectomy, right lateral nasal wall, and hard palate resection
|
Free VRAM with three debulking procedures
|
4 mo
|
Antonetti et al (2009)[14]
|
10/M
|
Burn
|
Mandibular resection and debridement
|
Free FOCF
|
10 mo
|
Ojeda-Uribe et al (2010)[16]
|
55/F
|
DM2
|
Debridement of lower lip and chin, mandibular and floor of the mouth resection with
partial glossectomy
|
Mandibular porous titanium prosthesis and LDFF
|
Late
|
Metzen et al (2012)[9]
|
63/F
|
MDS
|
Right infrastructure maxillectomy
|
SOFF
|
Immediate
|
Herford et al (2013)[7]
|
13/M
|
MDS
|
Anterior maxillectomy
|
LeFort I advancement and a two-stage tong flap
|
Late
|
Murphy et al (2013)[17]
|
68/M
|
MDS
|
Right orbital exenteration, resection of frontal, maxillary and ethmoidal sinuses,
and inferior and middle turbinates
|
Chimeric ALT–VL flap
|
2 wk
|
Silberstein et al (2014)[10]
|
41/F
|
DM2
|
Two interventions: left orbital exenteration, left subtotal maxillectomy, bilateral
ethmoidectomy, sphenoidectomy, partial rhinectomy, and right maxillary sinus antrostomy
|
Free TRAM + FTSG, and an STSG in a second stage
|
2 mo
|
Bhatnagar and Agarwal (2016)[12]
|
35/M
|
–
|
Right type IV orbital exenteration and medial orbital wall resection
|
RFFF
|
6 mo
|
Augustine et al (2017)[11]
|
2/M
|
MDS
|
Left total maxillectomy, resection of the hard palate, nasal septum and left ethmoid
sinus
|
Free FOCF + nasal strut
|
–
|
4.5/M
|
MDS
|
Four interventions: type II orbital exenteration, resection of facial muscles, external
ethmoidectomy, nasal and Caldwell–Luc resection
|
VIOF with 2 skin pads
|
8 mo
|
Abbreviations: ALT, anterolateral thigh; ARF, acute renal failure; DM2, diabetes mellitus
type 2; F, female; FOCF, fibula osteocutaneous flap; FTSG, full-thickness skin graft;
LDFF, latissimus dorsi free flap; LFCP, left femoral circumflex perforator; M, male;
MDS, Myelodysplastic syndrome; MOF, multi organic failure; MSAP, medial sural artery
perforator; RFFF, Radial forearm free flap; SAH, systemic arterial hypertension; SOFF,
scapula osteocutaneous free flap; STSG, split-thickness skin graft; TRAM, transverse
rectus abdominis musculocutaneous; VIOF, vascularized iliac osteocutaneous flap; VL,
vastus lateralis; VRAM, vertical rectus abdominis musculocutaneous.
Inclusion and Exclusion Criteria
Inclusion and Exclusion Criteria
From all of the selected original articles, we analyzed those patients who underwent
reconstructive surgery with a free or pedicle flap after surgical resection due to
head- and neck-related mucormycosis infections. Observational studies were included
(retrospective and prospective) in addition to case reports. Articles containing data
from other studies or duplicate studies were excluded in addition to review articles,
technical descriptions, discussions, commentaries, editorials, and letters. For articles
presented by the same author, we verified that data were not identical; if identical
data or if any doubt existed, the data were excluded. Data were extracted independently
by two researchers (EH and MAR), and disagreements were resolved by consensus with
the senior author (JP). The collected data included the author, publication date,
study location, patient age, sex, localization, comorbidities, medical treatment,
surgical resection, postsurgical complications, reconstruction and flap types, and
reconstruction and follow-up times.
Results
Five reconstruction cases in patients with head and neck mucormycosis were presented
([Table 1]); from those, four rhinocerebral and one cutaneous (case 1) infection were observed.
All of them were treated with L-AmB. Reconstruction was done immediately after surgical
resection and debridement in four cases, and in one case, we did a secondary reconstruction
5 weeks after surgical treatment. In one patient (case 2), two debridement surgeries
were done. Initially this patient had a craniectomy and 2 weeks later, a right orbital
exenteration and immediate reconstruction with a frontal flap was done. A second reconstruction
was done for the methyl methacrylate cranial prosthesis insertion. In all five flaps,
no complications were presented although one of our patients (case 1) died on the
10th day postoperatively due to nosocomial pneumonia, showing no signs of mucormycosis
recurrence, flap loss ([Fig. 2]), or adverse cerebral effects.
Fig. 2 Case 1: (A) Patient with extensive cutaneous mucormycosis. After complete resection of the affected
tissue, performing a left orbital exenteration, resection of the submandibular gland,
and left facial muscles (B) were reconstructed with a 22 cm × 16 cm anterolateral thigh (ALT) flap covering the
left hemifacial defect (c).
Case 4: A 17-year-old female with a 1-year history of diabetes was admitted for an oronasal
fistula ([Fig. 3A]), signs of chronic sinusitis, and periocular edema. L-AmB was initiated due to a
high suspicion of mucormycosis. After a week of antifungal treatment, the patient
presented with blurry vision. Thus, a mucosal biopsy of the right sinus was taken
and finding Rhizopus sp. was detected. The CT scan showed eye and ocular muscle involvement. Thus, a right-orbital
exenteration and total maxillectomy were done. Intraoperative analysis from the resected
tissue margins was reported as negative. Although hyphae invasion was reported in
the temporal receptor vein wall ([Fig. 1]), delayed reconstruction was chosen and the wound was covered with Acticoat (Smith
& Nephew, Hull, UK). Postoperatively, the patient presented with a nasoorbital and
oroantral fistulas ([Fig. 3B]) and continued with antifungal therapy for 5 weeks, additionally, until reconstructive
surgery was done. For surgical planning, we made a stereolithography model and repeated
the CT scan with bone reconstruction to analyze the extent of the bone defect and
the localization of the fistulas. A 12 cm × 7 cm medial sural artery perforator flap
was anastomosed to the facial artery, covering the nasoorbital and oroantral fistula.
The patient continues to be asymptomatic with no evidence of fistula or mucormycosis
up to the 2-month follow-up ([Fig. 3C]).
Fig. 3 Case 4: (A) Patient shown preoperatively with the oro-nasal fistula. (B) Posterior to the right orbital exenteration and total maxillectomy, a nasoorbital
(solid white arrow) and an oro-antral fistula (hollow white arrow) were presented.
(C) One month after reconstruction, the patient was satisfied with the final results
although the eye prosthesis is pending.
Case 5: A 46-year-old male with undiagnosed diabetes, was admitted after 1 week of progressive
eye pain and redness, progressed with fever, and presented with hard palate necrotic
eschar ([Fig. 4A]), ophthalmoplegia, proptosis, left eye vision loss, and cephalea. The CT scan revealed
eye involvement and partial infiltration of both maxillas and the left zygomatic bone.
Since the extension was large, MRI was performed to assess brain involvement, but
it was discarded as it only showed infiltration in the optic nerve. As such, a multidisciplinary
team performed a left orbital exenteration, total left and partial right maxillectomy,
and a partial ethmoidectomy ([Fig. 4B]). Most of the viable skin was spared in addition to a portion of the soft palate.
After a negative report for hyphae invasion from the specimen's margins and receptor
vessels (temporal vessels), reconstruction was immediately done with an 18 cm × 12 cm
chimeric anterolateral thigh (ALT) with vastus lateralis (VL) flap ([Fig. 4C–E]). The patient was admitted to the intensive care unit. The definitive report from
the pathologist was a M. sp. infection. On the 10th day, the patient presented significant clinical improvement
([Fig. 4F–G]). He was discharged in accordance with his wishes and did not present for his follow-up.
Fig. 4 Case 5: (A) Upon admission, the patient presented with a hard palate necrotic eschar in addition
to left eye involvement. (B) Patient after a left orbital exenteration, total left, and partial right maxillectomy,
partial ethmoidectomy. (C) The reconstruction was made with a chimeric ALT flap with a portion of vastus lateralis
muscle. The descending branch of the circumflex femoral artery entering the vastus
lateralis is revealed and giving three cutaneous perforators to the folded skin flap.
(D) Here is shown how that distal part of the muscle flap is suspended through a small
perforation in the superior roof of the right sinus. (E) The distal portion of the skin flap is sutured to the borders of the oral roof and
soft palate, the medial portion of the flap is de-epithelized, and a circular skin
island patch was left for adequate closure in the orbital defect. (F, G) After 2 weeks, a satisfactory flap closure in the oral roof was observed in addition
to the proper cheek projection despite a total maxillectomy and resection of the base
and left lateral nose wall.
In the literature review, we collected 16 cases from 14 different publications, being
the first one published from 1999. Reconstruction was made with a free flap (12/16)
or pedicled flaps[4]
[5]
[6]
[7] (4/16). All of the patients had a head and neck mucormycosis. With respect to all
of the cases, 15 were diagnosed as rhinocerebral and one case as cutaneous mucormycosis.[6] Eleven patients were males and five were females with a mean patient age of 33.0
years. Multiple etiologies were reported, such as diabetes mellitus was the cause
in five cases, myelodysplastic malignancies in five cases, trauma in three cases,
one case of burn injury, one patient had diabetes mellitus in addition to a myelodysplastic
malignancy, and finally, one patient without any etiology. Delayed reconstruction
after surgical debridement was employed in most cases (13/16) with an average time
of delayed reconstruction of 16.7 weeks (range: 2–36 weeks). Only two authors (3/16)
described early or immediate reconstruction.[8]
[9]
From the cases in our literature review, multiple complications were reported secondary
to delayed reconstruction. Among the 13 cases of delayed reconstruction, 9 presented
postsurgical complications in which fistula was detected as the most common complication.
Three of them were oronasal,[7]
[10]
[11] two were nasoorbital,[5]
[12] and one was oropharyngeal.[13] Moreover, various complications, such as recurrent bleed,[12] exposed meninges,[10] cerebrospinal fluid leak,[8] contractions of anterior neck,[14] and temporomandibular ankylosis[6] were reported. In all of these cases, L-AmB was used from the time when the infection
was suspected, and in four cases, it was used in conjunction with another antifungal
(voriconazole, fluconazole, posaconazole, or tobramycin).[11]
[15]
[16]
[17] The follow-up period presented a mean of 26.3 months (range: 1–72 months).
One study could not be added to our study since it had a lack of patient details and
described the use of a chimeric serratus anterior flap with the seventh rib for reconstruction
after a maxillectomy.[18] Besides head and neck reconstructions, other cases of microsurgical reconstruction
have been reported in patients with mucormycosis. Reinbold et al[19] published a report concerning a deep inferior epigastric perforator flap used to
cover a patient with an arm amputation and mastectomy. Kyriopoulos et al[20] described pedicle latissimus dorsi musculocutaneous and groin flaps for reconstruction
of upper extremity burns. Moran et al[21] used a latissimus dorsi free flap and an anterolateral thigh (ALT) flap for a patient
with upper extremity trauma. Aggarwal and Pennington[22] used an inferior gluteal artery free flap in addition to two transverse rectus abdominis
musculocutaneous (TRAM) flaps for buttocks reconstruction.
Discussion
The mucormycosis incidence in our hospital is increasing and undoubtedly the determining
factor encountered in our patients has been immunosuppression triggered by uncontrolled
or complicated diabetes mellitus. The global prevalence of diabetes in adults has
increased in the past 30 years, reaching 9.8% in men and 9.2% in women since 2008.[23] Mexico reached an overweight adult population of 71.2% with a prevalence of diabetes
of 14.4% in 2006, which is expecting to increase to 22.5% by 2050.[24] We do not know precisely how the incidence of mucormycosis has changed over the
years or in other parts of the world. However, our theory is that a sustained increase
in obesity and diabetes in Mexico is the origin of the growing incidence of mucormycosis;
therefore, the necessity for management protocols for these patients exists.
A prompt diagnosis is the most critical aspect of an improved outcome. Most cases
(> 90%) are confirmed by the time of the autopsy, and in 81% of the patients, the
autopsy was the only positive diagnostic tool.[25] It is known that diplopia, ophthalmoplegia, proptosis, ocular pain, periocular cellulitis,
acute vision loss, and nasoantral, or cutaneous eschars in a predisposed host carry
a potentially high-predictive value.[1] In a study of 292 cases, it was found that ophthalmoplegia, proptosis, cranial nerve
palsy, ocular involvement, peri and orbital cellulitis, and fever appeared to be imminent
indications of surgical debridement.[26] Since antifungal therapy could lead to atypical morphological features, thus reducing
the ability to differentiate mucorales from other filamentous fungi, a trained pathologist
should examine the specimens,[27] although a negative biopsy with progressive disease should never delay surgical
debridement. For adequate surgical planning, a CT scan is a fundamental tool in early
diagnosis of invasive infections, especially when assessing bone involvement. Although
a CT scan is not pathognomonic, the absence of one cannot exclude invasion.[1]
[27]
Along with L-AmB, radical surgical debridement must be expeditious to eradicate the
fungal reservoir by acting aggressively until bleeding tissue, bone, and periosteum
is well-perfused with the antifungal agent. Because of the invasive and vascular nature
of the mucor, it is difficult to deliver the antifungal therapy into the hypovascularized
tissue. Cosmetic and functional impairment must not be chosen over a complete and
adequate surgical excision.
The existing literature reveals contradictory views regarding patient management.
When block resections are made, exposed bone and mucosal structures often remain.
If these structures are not reconstructed immediately, they will suffer desiccation,
and in some cases, even necrosis, leading to atrophy and contraction that will hinder
any subsequent reconstructions. Besides, we consider it unnecessary to submit these
patients to the visual impact generated by the disfiguring postoperative deformities
([Fig. 5A–E]). Moreover, covering the area with a well-vascularized flap facilitates antifungal
perfusion to the exposed tissue borders and avoids additional complications, especially
fistulas, exposed dura, and secondary wound infections. It could be argued that by
doing an immediate reconstruction, a remnant microscopic infection could be missed,
thus perpetuating the disease leading to further flap invasion, or even flap loss.
Although we do not recommend immediate reconstruction when hemodynamic instability
is present (which we found rare in these patients), we recommend it when there is
evidence of important cellulitis or aggregated infections, when a complete resection
cannot be completed, or intraoperatory biopsy of wound margins and recipient's vessels
are not available.
Fig. 5 Case 3: (A) Patient presented with affection of the left eye and hard palate. (B, C) After a complete workup, a left orbital exenteration and total maxillectomy were
performed, (D) leaving the patient with disfiguring results and possible surgical comorbidities
that were resolved with an immediate reconstruction with a ALT flap leading to acceptable
results (E) after three weeks postoperatively.
The choice of flap is based on the defects' size. In patients with orbital exenteration,
we strongly suggest the use of a medial sural artery perforator (MSAP) flap because
of its thin, pliable nature and long pedicle. If orbital coverage is not performed
immediately, the tissue can granulate on its own, with the possibility of later covering
it with a skin graft. If a maxillectomy is also performed (regardless of an exenteration),
an ALT flap reconstruction is ideal because it offers adequate cover to the orbit,
cheek skin, and palate besides providing sufficient volume and projection to the malar
region. In our opinion, in those cases in which the eye is not preserved, it is unnecessary
to reconstruct the defect with an osteocutaneous flap. We recommend focusing on skin
coverage and volume.[28] In larger segments, the defect can be reconstructed using a chimeric ALT flap since
this type of flap offers a wide cutaneous island and provides a large volume when
accompanied with a vastus lateralis segment. The versatility of this flap is unparalleled
since you can design as many skin islands as there are perforators, and it can be
used with fascia and a large muscle segment.
When one-third of the palate and nasal floor is affected or oral reconstruction is
needed, reconstruction with a facial artery musculomucosal flap is ideal, whereas
we suggest the MSAP is used when a greater resection is needed.
Conclusion
The issue that should be resolved is whether to perform an immediate or delayed reconstruction
after complete resection. Thus, multicenter studies are required to determine the
impact on these patients. With deep resections, vital tissues are left exposed and,
if not covered, could increase these patients' morbidity and mortality. Secondary
reconstruction comes together with tissue atrophy and retraction leading to a higher
patient disfiguration which produces an impact on the patient and the family. Preventing
this type of impact is why we suggest aggressive treatment and always enforce immediate
reconstruction, which can be performed safely based on clinical criteria, and after
an intraoperative study of wound edges and recipient's vessels, also showing an absence
of hyphae invasion.