Keywords
gorham-stout disease - pregnancy - lung - treatment
Hellyver et al reported one year ago, an interesting case of Gorham-Stout Disease
(GSD) in a young female during pregnancy.[1] This case report helped us to manage a similar complex case of a young woman who
presented an acute onset of GSD in the 25th pregnancy week with unilateral lung involvement.
This rare lymphatic disorder generally occurs in children or young adults with no
predilection of sex.[2]
[3] It is generally associated with vanishing bone osteolytic lesions, and thoracic
and abdominal involvement with diffuse pulmonary lymphangiomatosis.[2] Chylous effusions and chylothorax, consequent to the abnormal proliferation of lymphatic
vessels may induce respiratory failure with a high mortality risk.[4]
[5]
[6] Extrapulmonary alterations may include chylous ascites, lymphopenia, and destructing
bone disease for overgrowth of lymphatic vessels.[4]
[5]
[6]
[7] The pathogenesis of the disease is unclear and the prognosis is related to disease
localizations. The therapeutic approach to this rare disease includes surgical procedures
(such as thoracic duct ligation for chylothorax, drainages, etc.), support therapies
(such as albumin transfusion, oxygen therapy, low-fat medium-chain triglyceride diets),
and pharmacological approaches (tamoxifen, interferon-α, radiation, systemic steroids,
hormones, oncologic drugs, somatostatin, bevacizumab, and sirolimus); however, no
drug has been correctly validated until now.[3]
[7]
[8]
[9]
[10]
[11]
[12] Bilateral lung transplantation can be a therapeutic option in selected cases.[11]
Case Presentation
Here, we report the case of a young woman who developed a severe and recalcitrant
GSD with persistent unilateral chylothorax during pregnancy. The complex management
of this patient during and after pregnancy was discussed and compared with literature
data to contribute to the definition of a correct diagnostic and therapeutic approach
to this rare disease. A 32-year-old African woman, in her 25th pregnancy week, was
admitted to our hospital referring acute dyspnea at rest and severe nocturnal orthopnea.
The patient had no fever or cough but she referred acute chest pain. She already had
three previous pregnancies without complications. Because of the dyspnea persistence
and the abolition of left lung breath sound on physical examination, a chest X-ray
was performed revealing left pleural effusion. The thoracentesis allowed the drainage
of 1900 cc of a milky fluid. The pleural fluid analysis consisted of chylothorax,
that unfortunately continued to re-form (more than 700 ml/day), requiring maintenance
of the drainage. An interdisciplinary meeting involving also the gynecologists was
organized to take a therapeutic decision, as the risk of surgery in that phase of
pregnancy was too high as well as the introduction of immunosuppressive pharmacological
drugs (at high risk for the fetus). In the 30th pregnancy week, ultrasounds revealed
an intrauterine growth retardation with flowmeter alterations. Thus, a caesarean delivery
was performed and a 1.8 kg baby girl was born. Placenta histology revealed minimal
focal inflammation of the membranes with numerous vessel ectasia of the chorionic
villi. The patient continued to discharge abundant milky fluid from her drainage,
and postpartum highresolution CT scans of the chest and abdomen were performed, revealing
diffuse interlobular and peribronchial septal thickening with left pleural effusion,
no mediastinal lymph node enlargement, but several mediastinal cysts ([Figs. 1]
[2]
[3]
[4]). The liver appeared enlarged, multiple cystic areas were observed in the spleen,
and abundant fluid groundwater was observed in the pelvic cavity and perirenal areas.
Multiloculated fluid density cysts in lomboaortic region were observed, as well as
rarefaction lesions of sternum and D12 vertebra. Antinuclear autoantobodies were positive
although, rheumatologic consultation did not reveal abnormalities; blood quantiferon
and microbiological cultures were negative as well as all serological biomarkers of
infection and albumin concentrations in serum were low. Unfortunately, the patient
continued to be tachypneic and tachycardic. The treatment strategy for pleural effusion
was established. Video-assisted thoracoscopic surgery (VATS) was performed for diagnostic
reason to do parietal pleural biopsies, and for therapeutic purposes to perform talc
pleurodesis with scarification. But the patient continued to deteriorate requiring
further surgical approach for lung decortication and diaphragmatic plication. This
last procedure was performed because the chylous was sparing from diaphragmatic pleurocysts
(resembling lymphangiomas) that were biopsied. The patient fasted for 10 days after
surgery receiving only total parenteral nutrition with a < 5 g oral fat diet followed
by a low-fat medium-chain triglyceride diet and octreotide injections. Microscopic
examination showed extensive acute and chronic inflammation of parietal and diaphragmatic
pleura with giant cells and proliferative lymphatic channels with angioectasia and
without cytological atypia. Reactive mesothelial hyperplasia was described, immunohistochemistry
for calretinin, CK7, CK5/6, Estrogen Receptor (ER) and Progesterone Receptor (PR)
testing was performed, and lymphatic vessels alterations were documented. The patient
was discharged with a diagnosis of GSD. Actually, she is alive, she has had a healthy
daughter but she needs specific treatments such as steroids, low-fat medium-chain
fat diet, and anti-inflammatory drugs for the persistence of dyspnea, chest pain,
and minimal pleural effusion.
Fig. 1 Small lytic lesions of the vertebra (D12), pelvis (right iliac wing), and stern um.
Fig. 2 Multiloculate cystic fluid density mass (lymphangiomas) in the anterior mediastinum.
Fig. 3 (A) Peribronchovascular and interlobular interstitial thickening and pleural thickening
in the left lung, and (B) Left chylous pleural effusions.
Fig. 4 Multiple, low attenuation, rounded lesions of the spleen.
Discussion
The features of this case include the onset of GSD during pregnancy, and the unilateral
chylothorax consequent to thoracic vertebrae and sternum involvement. In this pregnant
patient, the lymphatic invasion into the pleural cavity seems to be induced by bone
GSD involvement, hormonal stimuli, and by the increase of intra-abdominal pressure
associated with chylous ascites. The hormonal stimuli may have had a role as the patient
was in the 25th pregnancy week of her fourth pregnancy when she developed GSD, analogously
to a similar case published in your journal.[1] The main difference was that in the already published case, a prenatal diagnosis
of GSD was done many years ago and the woman developed an acute disease phase, with
severe recalcitrant chylothorax during the fourth pregnancy week; she was treated
using a more conservative approach compared to our patient, as the chylothorax was
discovered at the beginning of the pregnancy.[1] Hellyver and coauthors wondered about the possibility that female hormones produced
during pregnancy can trigger this exacerbation.[1]
[12] Perhaps, our case supports the suspicion that pregnancy may trigger chylothorax
in GSD together with changes in intrathoracic pressure, as suggested for idiopathic
chylothorax occurring during pregnancy.[10]
[12]
[13]
[14]
[15] No pathogenetic studies have been performed to verify the potential role of estrogens
in lymphatic alterations and bone cellular metabolism occurring in GSD during pregnancy.[1] In our patient as well as in the one previously described, low oral fat diet together
with total parenteral nutrition gave positive effects, while octreotide therapy proved
ineffective only in our patient and not in the other cases.[1]
[12]
[13]
[14]
[15]
In conclusion, the present case study illustrates an unusual presentation of GSD during
pregnancy underlining the difficulties in the management of this disease to guaranty
good fetal and mother evolution. Further studies are required to improve the limited
therapeutic options of this rare disease.
